GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Saccharomonospora cyanea NA-134

Align isocitrate dehydrogenase (NAD+) (EC 1.1.1.41) (characterized)
to candidate WP_005456797.1 SACCYDRAFT_RS13140 isocitrate dehydrogenase

Query= BRENDA::Q945K7
         (374 letters)



>NCBI__GCF_000244975.1:WP_005456797.1
          Length = 481

 Score =  258 bits (659), Expect = 2e-73
 Identities = 150/344 (43%), Positives = 210/344 (61%), Gaps = 12/344 (3%)

Query: 39  SSTTPITATLFPGDGIGPEIAESVKKVFTTAGVPIEWEEHYVGTEI-DPRTQSFLTWESL 97
           S++ PIT     GDGIGPEI E+   V   AG  ++ +   +G  +      + +T E+L
Sbjct: 5   STSAPITVA--HGDGIGPEIMEATLSVLNAAGAALDIDTITIGESVYQAGNPAGVTPEAL 62

Query: 98  ESVRRNKVGLKGPMATPIGKGHRSLNLTLRKELNLYANVRPCYSL-PGYKTRYDDVDLIT 156
           ES+RR  V LK P+ TP G G +SLN+T+RK   LYANVRPC +  P   T++  +D++ 
Sbjct: 63  ESIRRTGVFLKAPITTPQGGGFKSLNVTVRKTFGLYANVRPCVAYAPFVATKHPGMDVVI 122

Query: 157 IRENTEGEYSGLEHQVVRGVVESLKIITRQASLRVAEYAFLYAKTHGRERVSAIHKANIM 216
           +REN E  Y+G+EH+    VV+ LK+I+RQ   RV  YAF YA  + R +V+A  K NIM
Sbjct: 123 VRENEEDLYAGIEHRQTDEVVQCLKLISRQGCERVIRYAFEYATAYRRTKVTAFTKDNIM 182

Query: 217 QKTDGLFLKCCREVAEKYPEITYEEVVIDNCCMMLVKNPALFDVLVMPNLYGDIISDLCA 276
           + TDGLF +   EVA  YP+I  E  ++D     L   P  FDV+V+PNLYGDI+SD+ A
Sbjct: 183 KMTDGLFHRVFDEVAADYPDIQAEHWIVDIGAAKLADTPEAFDVVVLPNLYGDILSDVAA 242

Query: 277 GLVGGLGLTPSCNIGEDGVALAEAVHGSAPDIAGKNLANPTALLLSGVMMLRHLKFNEQA 336
            + G +GL  S NIGE  VA+ EA+HGSAP  AG+++ANP+ LLL+ V ML H+   + A
Sbjct: 243 QIAGSVGLAGSANIGE-RVAMFEAIHGSAPRRAGQDVANPSGLLLAAVQMLVHIGQADVA 301

Query: 337 EQIHSAIINTIAEGKYRTADLGGSST------TTEFTKAICDHL 374
            ++H+A + TI +G   T D+    T      TT F  ++ D L
Sbjct: 302 SRVHNAWLRTIEDG-IHTYDIYEPDTSTSKVGTTAFAASVIDRL 344


Lambda     K      H
   0.318    0.134    0.389 

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: 437
Number of extensions: 22
Number of successful extensions: 4
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: 374
Length of database: 481
Length adjustment: 32
Effective length of query: 342
Effective length of database: 449
Effective search space:   153558
Effective search space used:   153558
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 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