GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Oleispira antarctica RB-8

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_046007640.1 OLEAN_RS00755 branched-chain amino acid aminotransferase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000967895.1:WP_046007640.1
          Length = 331

 Score = 98.2 bits (243), Expect = 2e-25
 Identities = 90/309 (29%), Positives = 137/309 (44%), Gaps = 33/309 (10%)

Query: 15  VPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKSAKFLHYD- 73
           VP +  ++    H LHY +  F GL+      + G++ +FR+D + +R+S+S++ L    
Sbjct: 28  VPSDKLELHPGAHVLHYSSTCFEGLKAFK--HEDGSVNVFRMDANIERMSQSSELLSLPA 85

Query: 74  ISAEKIKEVIVDFV-----KKNQPDKSFYIRPLVYSS----GLGIAPRLHNLEKDFLVYG 124
           I+ +++ ++I D V     +   P  S YIRP    +    G   AP   +L     V  
Sbjct: 86  INKDQLAQMIKDAVGLYADEVPTPPGSMYIRPTHIGTEPAIGKAAAPTASSL---LYVLL 142

Query: 125 LEMGDYLAADGVSCRISSWYRQED--RSFPLRGKI-SAAYITSALAKTEAVESGFD-EAI 180
             +GDY        R+     +ED  R  P  G I S     SAL          + + I
Sbjct: 143 SPVGDYFTGGAKPLRL---LLEEDGMRCAPHMGMIKSGGNYASALGPISRARKECNADQI 199

Query: 181 LMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQRPIDK 240
           L    G V E    N  ++   +I+T   +   L G+TRDSILTIA D G+   +R    
Sbjct: 200 LFCPNGDVQETGAANFILIDGNEIITKALDSTFLHGVTRDSILTIARDAGMTVTERDFTV 259

Query: 241 SELM-----IADEVFLSGTAAKITPVKRI----ENFTLGGDRP--ITEKLRSVLTAVTEN 289
           +EL+        E  LSGTAA +TPV  +    + FT+G   P   T KLR  L  +   
Sbjct: 260 AELLERAKKPGTEAALSGTAAVLTPVGTLIHNGQEFTVGSGEPGETTNKLRQALNDIQWG 319

Query: 290 REPKYQDWV 298
           +      W+
Sbjct: 320 KAEDKYGWL 328


Lambda     K      H
   0.320    0.138    0.406 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 253
Number of extensions: 11
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 305
Length of database: 331
Length adjustment: 27
Effective length of query: 278
Effective length of database: 304
Effective search space:    84512
Effective search space used:    84512
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory