GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Pedobacter sp. GW460-11-11-14-LB5

Align cystathionine gamma-lyase (EC 4.4.1.1); cysteine-S-conjugate beta-lyase (EC 4.4.1.13) (characterized)
to candidate CA265_RS13080 CA265_RS13080 O-succinylhomoserine sulfhydrylase

Query= BRENDA::A2RM21
         (380 letters)



>FitnessBrowser__Pedo557:CA265_RS13080
          Length = 388

 Score =  270 bits (690), Expect = 5e-77
 Identities = 146/365 (40%), Positives = 219/365 (60%), Gaps = 11/365 (3%)

Query: 23  SVPIYQTSTYKQNGLGQPK-----EYE---YSRSGNPTRHALEELIADLEGGVQGFAFSS 74
           S PIY TS+YK     + +     E E   YSR  NP      E +  LEG   GFA ++
Sbjct: 24  SSPIYLTSSYKFEDAEEMRALFANEKEGNVYSRYSNPNTSEFIEKMCLLEGAEDGFATAT 83

Query: 75  GLAGIHAVLSLF-SAGDHIILADDVYGGTFRLMDKVLTKTGIIYDLVDLSNLDDLKAAFK 133
           G+A I      F   GDH++ +  V+G T +L+  V +  G+ +D  DL    D +A  K
Sbjct: 84  GMAAIFTTFGAFLKNGDHLVSSRSVFGSTHQLLTNVFSNWGVTFDYADLDKPQDWEALIK 143

Query: 134 EETKAIYFETPSNPLLKVLDIKEISAIAKAHDALTLVDNTFATPYLQQPIALGADIVLHS 193
             TK I+ ETPSNP + ++D++ +  +AK H+ L +VDN FATPYLQQPI  GA I +HS
Sbjct: 144 PNTKMIFVETPSNPGIDIIDLEFLGDLAKKHNVLLVVDNCFATPYLQQPIKFGAHISIHS 203

Query: 194 ATKYLGGHSDVVAGLVTTNSKELASEIGFLQNSIGAVLGPQDSWLVQRGIKTLALRMEAH 253
           ATKY+ G   V+ G++    + +A  IGF ++S G  L P ++W++ + ++TLA+RM+ H
Sbjct: 204 ATKYIDGQGRVLGGVILGTKELIADVIGFARHS-GPALSPFNAWILSKSLETLAIRMDRH 262

Query: 254 SANAQKIAEFLETSKAVSKVYYPGLNSHPGHEIAKKQMSAFGGMISFELTDE-NAVKDFV 312
             NA K+AE+LE    +  V YP L SHP ++IAKKQM   GG+++  +    +A + F+
Sbjct: 263 CENALKVAEYLEKHPKIKLVKYPFLPSHPQYDIAKKQMKQGGGIVTIVVEGGIDAARKFM 322

Query: 313 ENLSYFTLAESLGGVESLIEVPAVMTHASIPKELREEIGIKDGLIRLSVGVEAIEDLLTD 372
           + L  F+++ +L    S+   PA  TH+ + +E R E+GI+ G IRLS+G+E I D+L D
Sbjct: 323 DGLQMFSISANLADTRSIATHPATSTHSKLTEEQRNEVGIEQGSIRLSIGLEHINDILAD 382

Query: 373 IKEAL 377
           I++AL
Sbjct: 383 IEQAL 387


Lambda     K      H
   0.315    0.133    0.366 

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: 387
Number of extensions: 10
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: 380
Length of database: 388
Length adjustment: 30
Effective length of query: 350
Effective length of database: 358
Effective search space:   125300
Effective search space used:   125300
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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