GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Nostoc punctiforme PCC 73102 ATCC 29133; PCC 73102

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_012409012.1 NPUN_RS12335 isocitrate/isopropylmalate family dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000020025.1:WP_012409012.1
          Length = 363

 Score =  179 bits (455), Expect = 7e-50
 Identities = 122/330 (36%), Positives = 175/330 (53%), Gaps = 29/330 (8%)

Query: 2   AYRICLIEGDGIGHEVIPAARRVLEATGLPLEF-VEAEAGW---ETFERRGTSVPEETVE 57
           +YRI  I G+GIG EV+ A+ ++L+       F ++ + GW     FE+ G+  P+ T E
Sbjct: 8   SYRIVAIPGEGIGPEVVEASLKILQHVAKIQGFTLQVDYGWLGATAFEQLGSYFPQATTE 67

Query: 58  KILSCHATLFGAATSPTRKVPGFFGAIRYLRRRLDLYANVRPA--------KSRPVPGSR 109
                   +FGA +          G +  LR+  D + N+RP         KS   P   
Sbjct: 68  LCDGADGIVFGAVSQ---------GGLLELRKHFDFFCNLRPIRSVNSLLHKSSLRPEKI 118

Query: 110 PGVDLVIVRENTEGLYVEQERRYLD----VAIADAVISKKASERIGRAALRIAEGRPRKT 165
            G+D++IVRE   G+Y     R  D              +   RI R AL  A+ R R  
Sbjct: 119 QGLDILIVRELVSGIYFGPSGRSSDERGNYGYHTMRYYDEEIRRIARKALEQAQYR-RGL 177

Query: 166 LHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTNL 225
           L +AHK N LP      L  V+E A  FP V V+ ++VDN AMQ+V+ P+RFDVI+ +NL
Sbjct: 178 LTVAHKENALPHLHWTRL--VQEEATKFPNVIVEPMLVDNLAMQMVLNPQRFDVILASNL 235

Query: 226 LGDILSDLAAGLVGGLGLAPSGNI-GDTTAVFEPVHGSAPDIAGKGIANPTAAILSAAMM 284
            GDILSD+   LVG +GL  S ++  +   ++E +HG+APDIAG GIANP   + +  +M
Sbjct: 236 FGDILSDIGGALVGSIGLLGSASLNANGFGLYEAIHGTAPDIAGLGIANPLGTLGACVLM 295

Query: 285 LDYLGEKEAAKRVEKAVDLVLERGPRTPDL 314
           L   GE +AA+++  A D +L +G RT DL
Sbjct: 296 LQQWGEVQAAQQIIAAQDRILAKGYRTADL 325


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: 258
Number of extensions: 16
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: 363
Length adjustment: 29
Effective length of query: 305
Effective length of database: 334
Effective search space:   101870
Effective search space used:   101870
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 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