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_020174404.1 A3OQ_RS0105685 3-isopropylmalate dehydrogenase
Query= SwissProt::Q58991 (347 letters) >NCBI__GCF_000385335.1:WP_020174404.1 Length = 368 Score = 185 bits (470), Expect = 1e-51 Identities = 139/368 (37%), Positives = 194/368 (52%), Gaps = 43/368 (11%) Query: 3 KVCVIEGDGIGKEVIPEAIKILN-----ELGEFEIIKGEAGLECLKKYGNALPEDTIEKA 57 K+ ++ GDGIG EV+ E KI + FE KG G +G A+ + + A Sbjct: 5 KLLILPGDGIGVEVMAEVEKIAQWFTKEGIAAFEFEKGLVGGCAYDAHGKAISDSDVALA 64 Query: 58 KEADIILFGAITSPK----PGEVKNYKSPIITLRKMFHLYANVRPINNFGIGQLIGKIAD 113 + AD +L GA+ PK P +V+ ++ ++ LRK L+AN+RP + +AD Sbjct: 65 QAADAVLLGAVGGPKWDGVPYDVRP-EAGLLRLRKDMQLFANLRPAICYPA------LAD 117 Query: 114 YEFLNAK---NIDIVIIRENTEDLYVGRERLENDT------AIAERVITRKGSERIIRFA 164 L + +DI+I+RE T +Y G + D AI +V ERI R A Sbjct: 118 ASSLKRELVDGLDIMIVRELTGGVYFGEPKQIIDLGNGQRRAIDTQVYDTYEIERIARVA 177 Query: 165 FEYAIKNNRKKVSCIHKANVLRITDGLF---LEVFNEIKKHYNIEADDYLVDSTAMNLIK 221 FE A K R KV+ K NV++ GL + + + ++E + L DS M L++ Sbjct: 178 FELARKR-RNKVTSSEKHNVMK--SGLLWYETVIALHARDYKDVECEHQLADSLGMQLVR 234 Query: 222 HPEKFDVIVTTNMFGDILSDEASALIGGLGLAPSANIGD-------DKALFEPVHGSAPD 274 P++FDVIVT N+FGDILSD AS L G LG+ PSA++G+ KAL+EPVHGSAPD Sbjct: 235 RPKQFDVIVTDNLFGDILSDIASMLTGSLGMLPSASLGEVDQKTGQRKALYEPVHGSAPD 294 Query: 275 IAGKGIANPMASILSIAMLFDY-IGEKEKGDLIREAVKYCLINKKVTPDLGGD----LKT 329 IAGKGIANP+A I S M Y G E D I +A+ L T D+ G+ + T Sbjct: 295 IAGKGIANPIAMIASFGMALRYSFGLIEAADKIEKAISSVLDKGLRTADIKGEKGDAVST 354 Query: 330 KDVGDEIL 337 +GD IL Sbjct: 355 SQMGDAIL 362 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: 311 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: 347 Length of database: 368 Length adjustment: 29 Effective length of query: 318 Effective length of database: 339 Effective search space: 107802 Effective search space used: 107802 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.
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:
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