GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metY in Methylomonas methanica MC09

Align O-acetylhomoserine sulfhydrylase (EC:2.5.1.49) (characterized)
to candidate WP_013817327.1 METME_RS03045 O-succinylhomoserine sulfhydrylase

Query= reanno::Korea:Ga0059261_3194
         (402 letters)



>NCBI__GCF_000214665.1:WP_013817327.1
          Length = 393

 Score =  326 bits (836), Expect = 6e-94
 Identities = 167/377 (44%), Positives = 239/377 (63%), Gaps = 2/377 (0%)

Query: 19  TQAIRGGTARSEWGETSEALFLTSGYAYDCAGDAAARFSGDQQGMTYSRLQNPTVEMLEQ 78
           TQAIR G  R+   E S  +F TS Y ++ A  A+ RF+G Q G  YSR  NPTV   +Q
Sbjct: 13  TQAIRAGQRRTHEDEHSIPIFATSSYVFESAEQASLRFTGKQPGNIYSRFTNPTVSAFQQ 72

Query: 79  RIALLEGAEACRATASGMAAMTAALLCQLSAGDHLIGGRAAFGSCRWLTDTQLPKFGIET 138
           R+AL+E  E C A +SGMAA+ A  +  L AGDH++  R+ FG+          KFG+  
Sbjct: 73  RLALMERGERCLAFSSGMAAIMAVGMALLKAGDHVVCSRSVFGNTVLTFQNYFGKFGVAC 132

Query: 139 TVVDARDPQQFIDAIRPNTKVFFFETPANPTMDVVDLKAVCAIARERGIVTVVDNAFATP 198
             V   D   +  AI+PNT+  F ETP+NP +++ D++A+  IA   G + VVDN F TP
Sbjct: 133 DFVGLTDLSAWEAAIQPNTRFLFLETPSNPLIEIADIQALADIAHRHGCLLVVDNCFCTP 192

Query: 199 ALQRPMDFGADVVAYSATKMMDGQGRVLAGAVCGTEEFINNTLLPFHRNTGPTLSPFNAW 258
            LQ+P+  GAD+V  SATK +DG GR + GAV G+EE I   + P+ R  G ++SPFNAW
Sbjct: 193 VLQQPLALGADLVVQSATKFIDGHGRCVGGAVIGSEELIEKDIYPYLRTGGASMSPFNAW 252

Query: 259 VVLKGLETLDLRIQRQSENALKVARFLEGR--VPRVNFPGLPSHPQHNLAMSQMAAAGPI 316
           V L GLETL +R++   +NA  +A +LE +  + +V++PGL SH QH LA  Q +  G +
Sbjct: 253 VFLSGLETLAIRMKAHCDNAFTLAAWLETQPGIAKVHYPGLASHAQHELARRQQSHFGAV 312

Query: 317 FSIELDGGRTQAHGLLDALGLIDISNNIGDSRSLMTHPASTTHSGVAEDQRLLMGVGEGM 376
            S EL GG+ QA  L+DA  ++ I+ N+GD ++ +THPA+TTH  ++ + R   G+ +G+
Sbjct: 313 VSFELTGGKEQAWKLIDATRMLSITANLGDVKTTITHPATTTHGRLSPEARAEAGITDGL 372

Query: 377 LRLNVGLEDPEDLIADL 393
           +R++VGLE+ ED+ ADL
Sbjct: 373 VRVSVGLENIEDIKADL 389


Lambda     K      H
   0.319    0.134    0.396 

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: 390
Number of extensions: 8
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: 402
Length of database: 393
Length adjustment: 31
Effective length of query: 371
Effective length of database: 362
Effective search space:   134302
Effective search space used:   134302
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: 50 (23.9 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