GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Trichormus variabilis ATCC 29413

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate WP_011320730.1 AVA_RS20495 homocitrate synthase

Query= curated2:Q8TYM1
         (509 letters)



>NCBI__GCF_000204075.1:WP_011320730.1
          Length = 372

 Score =  296 bits (759), Expect = 6e-85
 Identities = 156/355 (43%), Positives = 222/355 (62%), Gaps = 2/355 (0%)

Query: 14  VRIFDTTLRDGEQTPGVALTPEEKLRIARKLDEIGVDTIEAGFAAASEGELKAIRRIARE 73
           + I DTTLRDGEQ  G+A   EEK+ IA  LD IGV  +E G  A    E ++I RIA+ 
Sbjct: 6   IHINDTTLRDGEQAAGIAFNVEEKIAIASLLDSIGVHELEVGIPAMGHEEAESITRIAKL 65

Query: 74  ELDAEVCSMARMVKGDVDAAVEAEADAVHIVVPTSEVHVKKKLRMDREEVLERAREVVEY 133
            L+A++    R    D+ A+++   D VH+ VP S++ +  K +  R+ VL++ R+ + +
Sbjct: 66  GLNAKLLGWNRANLSDIQASIDCGLDRVHVSVPVSDIQIAAKFKGQRQLVLDKLRDAINF 125

Query: 134 ARDHGLTVEISTEDGTRTELEYLYEVFDACLEAGAERLGYNDTVGVMAPEGMFLAVKKLR 193
           A D GL+V +  ED +R +  +L EV  +  E GA R  + DTVG++ P   +  V  L 
Sbjct: 126 ACDRGLSVSVGGEDSSRADESFLLEVAQSAQEWGAFRFRFCDTVGILDPTTTYKKVSHLV 185

Query: 194 ERVGEDVILSVHCHDDFGMATANTVAAVRAGARQVHVTVNGIGERAGNAALEEVVVVLEE 253
             +   +++ +H HDDFGMA ANT+A V+AGA  V+ TVNGIGERAGNA LEEVV+ L+ 
Sbjct: 186 SHLS--IVIEMHTHDDFGMALANTLAGVKAGAISVNTTVNGIGERAGNAPLEEVVMGLKY 243

Query: 254 LYGVDTGIRTERLTELSKLVERLTGVRVPPNKAVVGENAFTHESGIHADGILKDESTYEP 313
           LY + TGI T+RL E+S+LV + T   V P KA+VGEN F HESGIHA G+L++  TYEP
Sbjct: 244 LYDIPTGIDTKRLVEVSRLVSKATNFPVLPWKAIVGENTFAHESGIHAHGVLQNPITYEP 303

Query: 314 IPPEKVGHERRFVLGKHVGTSVIRKKLKQMGVDVDDEQLLEILRRLKRLGDRGKR 368
             PE VG ERR V+GKH G  ++   L+Q G+ +   ++  +L  ++    + KR
Sbjct: 304 FAPEDVGWERRLVVGKHSGRHLLLSVLEQHGITLGQAEIQSVLDAVRHQSVKTKR 358


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: 419
Number of extensions: 19
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: 509
Length of database: 372
Length adjustment: 32
Effective length of query: 477
Effective length of database: 340
Effective search space:   162180
Effective search space used:   162180
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 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