GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hicdh in Sulfurivirga caldicuralii DSM 17737

Align Homoisocitrate dehydrogenase; HICDH; Homo(2)-isocitrate/homo(3)-isocitrate dehydrogenase; Isohomocitrate dehydrogenase; IHDH; NAD-dependent threo-isohomocitrate dehydrogenase; EC 1.1.1.87; EC 1.1.1.- (characterized)
to candidate WP_074201047.1 BUQ81_RS03680 3-isopropylmalate dehydrogenase

Query= SwissProt::Q58991
         (347 letters)



>NCBI__GCF_900141795.1:WP_074201047.1
          Length = 357

 Score =  204 bits (518), Expect = 4e-57
 Identities = 136/341 (39%), Positives = 199/341 (58%), Gaps = 28/341 (8%)

Query: 3   KVCVIEGDGIGKEVIPEAIKILNELGE-----FEIIKGEAGLECLKKYGNALPEDTIEKA 57
           KV V+ GDGIG E+  +A+K+L  L +      E+ +   G       G+ LPE T++ A
Sbjct: 4   KVLVLPGDGIGPEITEQAVKVLKRLSDEGAIDIEMEEALVGGAAYDAEGSPLPESTMQLA 63

Query: 58  KEADIILFGAITSPKPGEVKNYKSP---IITLRKMFHLYANVRPINNFGIGQLIGKIADY 114
           +EAD IL GA+  P+  ++   K P   ++ LR    L+AN+RP        L  ++A  
Sbjct: 64  READAILLGAVGGPQYDDLPRDKRPEKGLLGLRSGLGLFANLRP------AMLYPQLAHA 117

Query: 115 EFLNAK---NIDIVIIRENTEDLYVGRER----LENDTAIAERVITRKGSE--RIIRFAF 165
             L  +    +DI+I+RE T  +Y G+ R    LEN             SE  RI   AF
Sbjct: 118 SSLKPEVVSGLDILIVRELTGGIYFGQPRGIRTLENGEREGFNTYVYSESEIKRIAHVAF 177

Query: 166 EYAIKNNRKKVSCIHKANVLRITDGLFLEVFNEIKKHY-NIEADDYLVDSTAMNLIKHPE 224
           + A K N KKV+ I K+NVL +T+ L+ EV  E+ K Y ++  +  LVD+ AM L++ P+
Sbjct: 178 QAAQKRN-KKVTSIDKSNVLEVTE-LWKEVVTEVAKDYPDVTLEHMLVDNAAMQLVRWPK 235

Query: 225 KFDVIVTTNMFGDILSDEASALIGGLGLAPSANIGDD-KALFEPVHGSAPDIAGKGIANP 283
           +FDV++T NMFGDILSDEAS L G +G+ PSA++ ++ K ++EP HGSAPDIAG+ IANP
Sbjct: 236 QFDVMLTGNMFGDILSDEASMLTGSIGMLPSASLNEENKGMYEPSHGSAPDIAGQDIANP 295

Query: 284 MASILSIAMLFDY-IGEKEKGDLIREAVKYCLINKKVTPDL 323
           +A+ILS AM+  Y +G +++   I +AV   L     T D+
Sbjct: 296 LATILSAAMMLRYSLGAEDQAARIEQAVSKVLDQGLRTADI 336


Lambda     K      H
   0.319    0.140    0.397 

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: 288
Number of extensions: 18
Number of successful extensions: 5
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: 347
Length of database: 357
Length adjustment: 29
Effective length of query: 318
Effective length of database: 328
Effective search space:   104304
Effective search space used:   104304
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