GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Maridesulfovibrio zosterae DSM 11974

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_027723059.1 H589_RS0116575 pyruvate carboxyltransferase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000425265.1:WP_027723059.1
          Length = 368

 Score =  191 bits (484), Expect = 5e-53
 Identities = 130/371 (35%), Positives = 193/371 (52%), Gaps = 9/371 (2%)

Query: 16  IFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASE-GELKAIRRIAREE 74
           + DTTLR+G Q  G     E + RIA  L +IGVD IE G+    +  EL        E+
Sbjct: 2   LIDTTLREGAQLFGAYFNLETRKRIASSLIKIGVDEIELGWVGQEKLSELVQYVSSIAED 61

Query: 75  LDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVVEYA 134
               V S  R  + D+ AA E   D ++I VP S++H++K+L  DR+ +L +    V  A
Sbjct: 62  TVLSVWSPCR--EKDILAAAELSVDRINIGVPVSDLHIEKRLSTDRKALLHKISAAVRTA 119

Query: 135 RDHGLT-VEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKKLR 193
           +  G   V +  ED +R ++++           GA R+  +D++G + P  M   V K R
Sbjct: 120 KAVGFKYVSVGMEDVSRADIDFALTTALLAKACGASRIRLSDSLGQLTPRAMEKLVTKFR 179

Query: 194 ERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVLEE 253
            ++  D+  +VHCHDDFGMATAN V A+ +GA     +V GIGERAG A  EE+V  L  
Sbjct: 180 SQINIDI--AVHCHDDFGMATANAVTALESGAMYADCSVLGIGERAGIAVTEELVAWL-A 236

Query: 254 LYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTYEP 313
           L   +    T+ L ++  +V   + V VP  KAVVG + F  ESG+H   + K    +EP
Sbjct: 237 LRDSNDRYSTKVLKDVCLMVSAASKVHVPRTKAVVGTDIFACESGLHTHALSKLPELFEP 296

Query: 314 IPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKR-ITEA 372
             PE VG  R+  +G   G + +R  L   GVD     L  +   +++L  R +R +T +
Sbjct: 297 YNPESVGIFRKLAVGGKSGKAAVRSALDDCGVDCAATDLTTLTEAVRQLSCRLERPLTRS 356

Query: 373 D-LRAIAEDVL 382
           + L+   E+VL
Sbjct: 357 EFLKLNDEEVL 367


Lambda     K      H
   0.315    0.134    0.367 

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: 372
Number of extensions: 18
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: 509
Length of database: 368
Length adjustment: 32
Effective length of query: 477
Effective length of database: 336
Effective search space:   160272
Effective search space used:   160272
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: 51 (24.3 bits)

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