GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Phyllobacterium endophyticum PEPV15

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_106718830.1 CU100_RS22300 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_003010935.1:WP_106718830.1
          Length = 358

 Score =  208 bits (529), Expect = 2e-58
 Identities = 139/352 (39%), Positives = 195/352 (55%), Gaps = 25/352 (7%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEATG-----LPLEFVEAEAGWETFERRGTSVPEETVE 57
           Y+I  I GDGIG EV+ A  RVLEA         L+  +   G + ++  G  +PE  ++
Sbjct: 4   YKIAAIPGDGIGKEVVAAGLRVLEACSSRDGNFKLDVADFPWGSDYYKAHGVLMPEGGID 63

Query: 58  KILSCHATLFGAATSPTRKVPG---FFGAIRYLRRRLDLYANVRPAKSRP-VPGSRPGV- 112
           ++ +  A  FGA  +P   VP     +G    + +  D YANVRP +  P +     GV 
Sbjct: 64  ELKAFDAIYFGAVGAPD--VPDHLTLWGLRLAICQPFDQYANVRPTRILPGIESPLRGVT 121

Query: 113 ----DLVIVRENTEGLYVEQERRYL-----DVAIADAVISKKASERIGRAALRIAEGRPR 163
               D VIVREN+EG Y  Q  R       +VA   ++ ++    RI R A ++A+ RPR
Sbjct: 122 ARDLDWVIVRENSEGEYAGQGGRSHRGLPEEVATEVSIFTRAGVSRIMRFAFQLAQSRPR 181

Query: 164 KTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTT 223
           K L +  K+N       L+ +  +EVA DFP V    ++VD   +++ + P   D IV T
Sbjct: 182 KLLTVVTKSNAQRHGMVLWDEIAREVANDFPDVIWDKMLVDAMTVRMTLNPGSLDTIVAT 241

Query: 224 NLLGDILSDLAAGLVGGLGLAPSGNI---GDTTAVFEPVHGSAPDIAGKGIANPTAAILS 280
           NL  DILSDLAA L G +G+AP+ N+   G   ++FEP+HGSA DI GKGIANP     S
Sbjct: 242 NLHADILSDLAAALAGSIGIAPTANLNPEGRFPSMFEPIHGSAFDITGKGIANPVGTFWS 301

Query: 281 AAMMLDYLGEKEAAKRVEKAVDLV-LERGPRTPDLGGDATTEAFTEAVVEAL 331
           A MML++LGE  AA R+ +A++ V  +    TPDL G+ATTE  T+AV  A+
Sbjct: 302 AVMMLEHLGEASAAARLMRAIERVTADPALHTPDLRGNATTEMVTQAVCAAI 353


Lambda     K      H
   0.319    0.137    0.391 

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: 279
Number of extensions: 20
Number of successful extensions: 7
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: 334
Length of database: 358
Length adjustment: 29
Effective length of query: 305
Effective length of database: 329
Effective search space:   100345
Effective search space used:   100345
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Jul 26 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