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On this page

This site covers with . Version information .

An attribute directive changes the appearance or behavior of a DOM element.

attribute

Try the live example ( view source ) .

There are three kinds of directives in Angular:

Components are the most common of the three directives. You saw a simple component in the Free Shipping Best Wholesale Alaïa Suede ZipperAccented Boots Browse Clearance Cheap Price T7JkvT
.

Structural Directives change the structure of the view. Two examples are NgFor and NgIf . Learn about them in the Structural Directives page.

Attribute directives are used as attributes of elements. The built-in NgStyle directive in the Ballet pumps black Clearance Countdown Package Free Shipping Visa Payment Sale Comfortable AVRLMz
page, for example, can change several element styles at the same time.

There are two kinds of attribute directive:

Creating a class-based attribute directive requires writing a controller class annotated with @Directive() , which specifies the selector that identifies the attribute. The controller class implements the desired directive behavior.

This page demonstrates building a simple myHighlight attribute directive to set an element’s background color when the user hovers over that element. You can apply it like this:

Follow the setup instructions for creating a new local project named attribute_directives .

Create the following source file in the indicated folder:

@Directive() requires a CSS selector to identify the HTML in the template that is associated with the directive. The CSS selector for an attribute is the attribute name in square brackets. Here, the directive’s selector is [myHighlight] . Angular locates all elements in the template that have an attribute named myHighlight .

Why not call it “highlight”?

Though is a more concise name than and would work, a best practice is to prefix selector names to ensure they don’t conflict with standard HTML attributes. This also reduces the risk of colliding with third-party directive names.

Make sure you do not prefix the directive name with because that prefix is reserved for Angular and using it could cause bugs that are difficult to diagnose. For a simple demo, the short prefix, , helps distinguish your custom directive.

After the @Directive() metadata comes the directive’s controller class, called HighlightDirective , which contains the logic for the directive.

Figure 1

Phylogeny and divergence timescales of mammalian species whose DPP sequences were compared . The phylogenetic and divergence time estimates are compilations of results reported in other molecular genetic studies and were based on genes other than [ 22 , 23 , Valentino 1975 Rockstud Sandals Low Shipping Fee Cheap Price Pay With Paypal sSGOt2
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Figure 2

Alignment of DPP's deduced amino acid sequences from the BMP1-cleavage domain through the RGD/vestigial integrin-binding motifs . (A) Note the conservation of the BMP1/tolloid-related protease cleavage domain (MQXDD). The underlined MQGDDP sequences were directly encoded by the 5' PCR primer during the production of an amplicon for that species. Due to direct sequencing of the original amplicon, only a portion of the bat sequence was available. The conserved RGD domains (red) are aligned with the vestigial tripeptides (bold). (B) In addition to the loss of their original RGD domains, the platypus was found to contain an RGD domain in a portion of DSP while the common shrew had two RGD motifs within DPP and 5' to the stop codon (*).

For the other 13 mammalian species in this study, the sequences encoding the MQGDD motif were directly the result of the 5' primer used in making the PCR amplicon (underlined in Figure 2A ). Therefore without verification by an independent sequencing reaction, these 13 species cannot be used to query the identity of the amino acid in the "X" position. The 8 species whose genomic DNA templates did not result in amplicons may have been the result of: 1) synonymous changes that would affect priming but not coding; 2) nonsynonymous changes that affect both priming and coding; or 3) completely missing BMP1-cleavage and/or end-of-translation motifs. The high degree of conservation of the BMP1-cleavage motif at the protein level in all studied DSPP sequences, however, does suggest that separation of the two domains (DSP and DPP) is important to their proper physiological functions in at least one critical tissue throughout the class of mammals. By comparison, the BMP1 cleavage domain in several species' DMP1 sequences predominantly had another relatively small amino acid, serine (S), for the "X" in the motif but other species had the glycine seen in DSPP as well as the large polar amino acid, asparagine (N) (data not shown).

The RGD tripeptide is one of the major defining motifs of the SIBLING gene family and its presence is necessary but not always sufficient for interaction with specific integrins including αvβ3, αvβ5, αvβ6, αvβ1, α5β1, and α8β1 [ 34 ]. For example, an intact RGD within both DMP1 and osteopontin (OPN) was necessary for supporting in vitro attachment of specific types of cells expressing αvβ3 integrins while another SIBLING, bone sialoprotein (BSP), was found to support such RGD-dependent attachment through either αvβ3 or αvβ5 integrins [ 7 ]. Changing the RGD into the chemically similar KAE amino acids destroyed these interactions. Interestingly, OPN's ability to effectively use the α9β 1 integrin remained cryptic until thrombin cleaved this SIBLING at a highly conserved site near the RGD domain [ 35 ]. It is not known at this time if the RGD motif of intact human DSPP can interact with any one or a subset of the RGD-dependent integrins and support cell attachment in vitro . It will also be interesting to eventually see if the integrin specificity of such interactions (if any) can be modified by cleavage at the BMP1 site.

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