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_106717507.1 CU100_RS15545 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_003010935.1:WP_106717507.1
          Length = 357

 Score =  221 bits (562), Expect = 3e-62
 Identities = 142/352 (40%), Positives = 202/352 (57%), Gaps = 24/352 (6%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEATGLPLEFVEAE-----AGWETFERRGTSVPEETVE 57
           Y I +IEGDGIG EVIP   RVLEA      F   +     A  + + R G  +PE   E
Sbjct: 6   YDIAVIEGDGIGKEVIPEGIRVLEAAARRHGFTLRQKWHDFAHCDYYARHGRMMPENWKE 65

Query: 58  KILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAKSR-----PVPGSR 109
           +I    A  FGA   P   VP     +G++   RR  D Y N+RP +       P+ G R
Sbjct: 66  EIGKPAAIFFGAVGWPDI-VPDHISLWGSLLQFRREYDQYVNLRPVRLMDGVPCPLSGRR 124

Query: 110 PG-VDLVIVRENTEGLYVEQERRYLD-----VAIADAVISKKASERIGRAALRIAEGRPR 163
           PG +D  +VRENTEG Y     R  +     + + + V+++K  +RI + A  +A+ RPR
Sbjct: 125 PGDIDFWVVRENTEGEYSAIGGRMFEGTEREMVMQETVMTRKGVDRILKFAFDLAQTRPR 184

Query: 164 KTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTT 223
           K +  A K+N + +T   + + V+ +A  +P V+     +D      V++P+ FDV+V +
Sbjct: 185 KLVTSATKSNGIAITMPYWDERVEAMASSYPEVSWNKFHIDILTANFVLKPQIFDVVVGS 244

Query: 224 NLLGDILSDLAAGLVGGLGLAPSGNI---GDTTAVFEPVHGSAPDIAGKGIANPTAAILS 280
           NL GDILSDL     G +G+APSGNI   G+  ++FEPVHGSAPDIAG+ +ANP   I S
Sbjct: 245 NLFGDILSDLGPACAGTIGIAPSGNINPEGEHPSLFEPVHGSAPDIAGRNLANPIGQIWS 304

Query: 281 AAMMLDYLGEKEAAKRVEKAVDLVLER-GPRTPDLGGDATTEAFTEAVVEAL 331
           AAMMLD+LGEK+AA  +  A+++VL++   RT DLGG A T+   +A+ + L
Sbjct: 305 AAMMLDHLGEKQAAADIMGAIEMVLKQPSLRTRDLGGAADTQTCGKAIADLL 356


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: 303
Number of extensions: 17
Number of successful extensions: 6
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: 357
Length adjustment: 29
Effective length of query: 305
Effective length of database: 328
Effective search space:   100040
Effective search space used:   100040
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