GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Rhodobacter sphaeroides ATCC 17029

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_011842036.1 RSPH17029_RS15290 tartrate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000015985.1:WP_011842036.1
          Length = 357

 Score =  218 bits (556), Expect = 1e-61
 Identities = 142/351 (40%), Positives = 200/351 (56%), Gaps = 24/351 (6%)

Query: 4   RICLIEGDGIGHEVIPAARRVLEATG----LPLEFVEAE-AGWETFERRGTSVPEETVEK 58
           +I +I GDGIG EV+P   RVLEA      + L F E + A  + + R G  +P++  E+
Sbjct: 7   KIAVIAGDGIGKEVVPEGLRVLEAVAGRHRIDLRFEEFDFASCDYYARHGQMMPDDWQER 66

Query: 59  ILSCHATLFGAATSPTRKVP---GFFGAIRYLRRRLDLYANVRPAK-----SRPVPGSRP 110
           +    A  FGA   P   VP     +G++   RR+ D Y N+RPA+       P+ G  P
Sbjct: 67  VGGHDALFFGAVGWPAT-VPDHVSLWGSLIQFRRQFDQYVNLRPARLMPGVPSPLAGRGP 125

Query: 111 G-VDLVIVRENTEGLYVEQERRYL-----DVAIADAVISKKASERIGRAALRIAEGRPRK 164
           G +D+ IVRENTEG Y     R       ++ + + V+S+   +R+ R A  +A  R R+
Sbjct: 126 GDIDMWIVRENTEGEYSAIGGRMYPGTEREIVLQETVMSRHGIDRVLRYAFELANRRERR 185

Query: 165 TLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVIVTTN 224
            L  A K+N + +T   + + V+ +A+D+P V      +D  A   V+ P+RFDV+V +N
Sbjct: 186 RLTSATKSNGISITMPYWDERVEAMAQDYPDVAWDKYHIDILAAHFVLNPDRFDVVVASN 245

Query: 225 LLGDILSDLAAGLVGGLGLAPSGNIGDTTA---VFEPVHGSAPDIAGKGIANPTAAILSA 281
           L GDILSDL     G +G+APSGNI    A   +FEPVHGSAPDIAG+GIANP   I + 
Sbjct: 246 LFGDILSDLGPACTGTIGIAPSGNINPERAFPSLFEPVHGSAPDIAGQGIANPVGQIWAG 305

Query: 282 AMMLDYLGEKEAAKRVEKAVDLVL-ERGPRTPDLGGDATTEAFTEAVVEAL 331
           AMML++LG  EAA  +  A++ VL +   RT DL G A T    +A+VEAL
Sbjct: 306 AMMLEHLGHAEAAAEIMAAIERVLADPRLRTRDLAGAADTVTCGKAIVEAL 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: 342
Number of extensions: 16
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: 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 Apr 10 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