GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Desulfotomaculum ruminis DSM 2154

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_013841352.1 DESRU_RS06675 homocitrate synthase

Query= curated2:O26819
         (496 letters)



>NCBI__GCF_000215085.1:WP_013841352.1
          Length = 377

 Score =  321 bits (823), Expect = 2e-92
 Identities = 170/370 (45%), Positives = 245/370 (66%), Gaps = 2/370 (0%)

Query: 2   QVRVLDTTLRDGEQTPGVSLTPEEKLRIALKIDALGADIIEAGSAITSEGEREGIRKITS 61
           ++ ++DTTLRDGEQT GV     EK+RIA  +D +G D IEAG  +    E+E I++I  
Sbjct: 5   KIWIVDTTLRDGEQTAGVVFANREKVRIASFLDEMGVDQIEAGVPVMGGDEQEAIKQICQ 64

Query: 62  EGLRAEICSFARAVREDIDAAISCDVDSVHLVVPTSDLHLEHKLRKTREEVLEQAVDCTE 121
            GL+A +  + R V +DI+A++ C VD+V + + TSD+H++HKL+ +RE V+E  V  TE
Sbjct: 65  LGLKASVMGWNRPVLKDIEASLKCGVDAVAISISTSDIHIKHKLKTSREWVVEHMVRATE 124

Query: 122 YAVDHGILVELSAEDSTRSDMDFLRTIFREGIEAGAERICACDTVGILTPERSYEFYRGL 181
           +A   G+ + ++AED++RSDM+FL    +   +AGA+R+  CDTVGIL P  +YE  + L
Sbjct: 125 FAKKEGMYISVNAEDASRSDMNFLIEFAKAAKQAGADRLRYCDTVGILEPFTTYERIKAL 184

Query: 182 SE-LGAPLSVHCHNDFGLAVANSLAGLRAGASEVHATINGIGERAGNAALEEVVVALKSL 240
            E +   + +H HNDFG+A AN+LAG+RAGA+ V  TI G+GERAGN+ LEEVV+ALK L
Sbjct: 185 KEAVDLEVEMHTHNDFGMATANALAGVRAGANWVGVTIMGLGERAGNSPLEEVVMALKHL 244

Query: 241 YDVDTSINIEMLYETSRMVARMTGVYLQPNKAIVGENAFAHESGIHADGVLKKAETYEPI 300
           YD+D S   E+  E +  V+R +G  L  +KAIVG N FAHESGIHADG +K  +TYE  
Sbjct: 245 YDIDLSFKTEIFREVAEYVSRASGRELHCSKAIVGSNMFAHESGIHADGAIKNPKTYEAF 304

Query: 301 TPEMVGHGRGFVMGKHIGTHALRKRLDELGMKVADDKLMEIFRRVKTLG-DMGKCVTDVD 359
            PE VG  R  V+GKH GT +LR +  E G+ +A ++  E+  ++++    + + + D +
Sbjct: 305 QPEEVGLERQIVIGKHSGTASLRMKFAEYGIDLAKEEAEELLPKIRSAAVSLKRSLFDKE 364

Query: 360 LQAIAEDVLG 369
           L  I ED  G
Sbjct: 365 LVYIYEDHFG 374


Lambda     K      H
   0.317    0.135    0.373 

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: 521
Number of extensions: 20
Number of successful extensions: 2
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: 496
Length of database: 377
Length adjustment: 32
Effective length of query: 464
Effective length of database: 345
Effective search space:   160080
Effective search space used:   160080
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 10 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