GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Hippea alviniae EP5-r

Align homoisocitrate dehydrogenase (EC 1.1.1.87) (characterized)
to candidate WP_022670320.1 G415_RS0104080 3-isopropylmalate dehydrogenase

Query= BRENDA::Q5SIJ1
         (334 letters)



>NCBI__GCF_000420385.1:WP_022670320.1
          Length = 361

 Score =  224 bits (570), Expect = 3e-63
 Identities = 146/347 (42%), Positives = 203/347 (58%), Gaps = 28/347 (8%)

Query: 3   YRICLIEGDGIGHEVIPAARRVLEATGL----PLEFVEAEAGWETFERRGTSVPEETVEK 58
           ++I + EGDGIG EV+    +VL+  G       E+ +   G    ++    +P+  VEK
Sbjct: 4   FKIAVAEGDGIGPEVVAEGLKVLDEVGSRFGHEFEYEKVYIGGCAVDKFEDPLPDSEVEK 63

Query: 59  ILSCHATLFGAATSPT-----RKVPGFFGAIRYLRRRLDLYANVRPAK--------SRPV 105
           IL C A  FGA   P      R+     G ++ +R+ L+ +AN+RPAK        S   
Sbjct: 64  ILKCDALFFGAVGGPKWDNLPREKRPETGMLK-IRKTLNAFANLRPAKVFDELVDASTLK 122

Query: 106 PGSRPGVDLVIVRENTEGLYVEQ-----ERRYLDVAIADAVISKKASERIGRAALRIAEG 160
           P    G+D+++VRE T G+Y  Q     E   +   I   + ++   ERI R A  +A  
Sbjct: 123 PEVIKGIDILVVRELTGGIYFGQPKGIVEENGVKKGINTMIYTEPEIERIVRLAFELARQ 182

Query: 161 RPRKTLHIAHKANVLPLTQGLFLDTVKEVAKDFPLVNVQDIIVDNCAMQLVMRPERFDVI 220
           R RK L    KANVL ++Q L+ D V++VAKD+P V    ++VDN AMQLV  P++FDVI
Sbjct: 183 R-RKKLTSVDKANVLDVSQ-LWRDVVEKVAKDYPDVEYNHLLVDNAAMQLVRDPKQFDVI 240

Query: 221 VTTNLLGDILSDLAAGLVGGLGLAPSGNIGDTTAVFEPVHGSAPDIAGKGIANPTAAILS 280
           VT N+ GDILSD A+ L G +G+ PS +IG    +FEP+HGSAPDIAG GIANP A I S
Sbjct: 241 VTGNIFGDILSDEASMLTGSIGMLPSASIGGEVGMFEPIHGSAPDIAGLGIANPIAQIES 300

Query: 281 AAMMLDYLGEK--EAAKRVEKAVDLVLERGPRTPDLGGDATTEAFTE 325
           AAMML Y G K  + A+ +EKAVD++L+ G RTPD+  + T +  T+
Sbjct: 301 AAMMLKY-GFKLDKEAEAIEKAVDMILKMGYRTPDIYSEGTRKVNTQ 346


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: 318
Number of extensions: 13
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: 361
Length adjustment: 29
Effective length of query: 305
Effective length of database: 332
Effective search space:   101260
Effective search space used:   101260
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.

Links

Downloads

Related tools

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