GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ofoA in Paucidesulfovibrio gracilis DSM 16080

Align 2-oxoacid:ferredoxin oxidoreductase subunit alpha; OFOR; EC 1.2.7.11 (characterized)
to candidate WP_078716536.1 B5D49_RS04770 2-oxoacid:acceptor oxidoreductase subunit alpha

Query= SwissProt::P72578
         (632 letters)



>NCBI__GCF_900167125.1:WP_078716536.1
          Length = 383

 Score =  159 bits (403), Expect = 2e-43
 Identities = 121/396 (30%), Positives = 199/396 (50%), Gaps = 26/396 (6%)

Query: 225 KERRRFWLDGNTAVAIGKIYGGVRFQSYYPITPASDESVYIEAHQDVLMEDPITGDKKKG 284
           K+R+  +  GN AV  G +  G  F   YPITP+S+           +ME       K  
Sbjct: 7   KKRKELFAQGNEAVVEGALLAGCSFYGGYPITPSSE-----------IMEGMAQRLPKTE 55

Query: 285 TIVVVQAEDELAAINMAIGAALTGVRAATATSGPGFSLMVEGLGWAGMNEVPVVITYYIR 344
           T   +Q EDE+A++   IGA+L G +A TATSGPGFSLM E LG+A M E P+V+   +R
Sbjct: 56  TGTFLQMEDEIASMGAVIGASLAGCKAMTATSGPGFSLMQEHLGYACMVEAPLVLVNVMR 115

Query: 345 GGPSTGLPTRTAQSDLIFPIFAGHGEFPKIVLASGDHAEAFKDAIWALNLAEKYQTPVIH 404
           GGPSTGLPT  AQ D+    +  HG+   +VL++ +  E  +  I A NLAEK++TPVI 
Sbjct: 116 GGPSTGLPTSPAQGDVQQARWGTHGDHAILVLSASNVQECLEMTITAFNLAEKFRTPVIL 175

Query: 405 LVEKTLANSYS--TIPYEELELDKLKAERGKIVESGDISYKRFKFTEDGISPRAFLGKAT 462
           L+++  A++     IP E    D+ +     +       YK F+ T  G+ P   +G   
Sbjct: 176 LLDEITAHTREKIVIPRE----DEYEVFNRVVPTMPPEWYKPFEETVRGVPPMPPIGSGY 231

Query: 463 MYY-TGDEHNEEGHISEDVVNRTMMYEKRMKKLEVADKEIPEESRVKIYGDLNSRNLIIT 521
            ++ TG  H+  G  +        + ++  +K+   D+ +P+ S  + +   ++   ++ 
Sbjct: 232 RFHVTGLTHDPNGFPTSRPEEVADLMDRMFRKV---DQFLPQVSLHEEFRCEDAEVCVVA 288

Query: 522 WGSPTGVLRDILE---ESNFDFTLLQIRMFSPFPKNLVSKLMEGRDKIITVEGNYLAQTS 578
           +GS        +E   E      LL+++   P+P+    K+M     +I  E N + Q S
Sbjct: 289 YGSVARSAEYAVEQARERGVKAGLLKLKTLYPYPRAATEKVMGHARALIVPEMN-MGQIS 347

Query: 579 LLVK-MYTGKDVTNSILKWNGRPFLRDELEEALIKV 613
             VK +  G+    ++ + +G+     E+ +A+++V
Sbjct: 348 REVKRVNNGRTTVRAVNRVDGQIITPSEILKAIMQV 383


Lambda     K      H
   0.316    0.135    0.382 

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: 484
Number of extensions: 21
Number of successful extensions: 3
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: 632
Length of database: 383
Length adjustment: 34
Effective length of query: 598
Effective length of database: 349
Effective search space:   208702
Effective search space used:   208702
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: 41 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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