Align 3-isopropylmalate/3-methylmalate dehydrogenase; 3-isopropylmalate dehydrogenase; 3-IPM-DH; IMDH; IPMDH; Beta-IPM dehydrogenase; D-malate dehydrogenase [decarboxylating]; EC 1.1.1.85; EC 1.1.1.n5; EC 1.1.1.83 (characterized)
to candidate WP_013706269.1 DESAC_RS06465 isocitrate dehydrogenase (NADP(+))
Query= SwissProt::Q58130 (333 letters) >NCBI__GCF_000195295.1:WP_013706269.1 Length = 416 Score = 164 bits (416), Expect = 3e-45 Identities = 124/365 (33%), Positives = 175/365 (47%), Gaps = 59/365 (16%) Query: 4 ICVIEGDGIGKEVVPATIQVLE-----ATGLPFEFVYAEA--GDEVYKRTGKALPEETIE 56 I IEGDG G ++ AT++VL+ A G V+ EA G++ Y+ G LPEET++ Sbjct: 28 ILYIEGDGTGPDIWRATVRVLDGAVARAYGGRRRIVWREALAGEKAYEAVGSHLPEETLK 87 Query: 57 TALDCDAVLFGA----AGETAADVIVKLRHILDTYANIRPVKAYKGVKC--LRPD-IDYV 109 + L G G + V LR +LD YA IRPV+ Y G P+ + V Sbjct: 88 AIKEYLVALKGPLTTPVGGGFRSINVTLRQVLDLYACIRPVRYYAGTPSPLREPEKTNMV 147 Query: 110 IVRENTEGLYKGIE--AEIDEGITIATRVITEKAC------------------ERIFRFA 149 I RENTE +Y GIE A+ E + + T+ C +R+ R A Sbjct: 148 IFRENTEDVYAGIEWPAQSSEARKVVNFLNTQMGCHISPEAGIGIKPMSAAGSQRLVRKA 207 Query: 150 FNLARERKKMGKEGKVTCAHKANVLKLTDGLFKKIFYKVA---------------EEYDD 194 A + + VT HK N++K T+G FK Y++A E+D Sbjct: 208 IIFALQTGRPS----VTLMHKGNIMKYTEGAFKTWGYELAAAEFKDRVITEEQLWREFDG 263 Query: 195 ------IKAEDYYIDAMNMYIITKPQVFDVVVTSNLFGDILSDGAAGTVGGLGLAPSANI 248 I +D D++ ++ +P+ + V+ T NL GD LSD A VGGLG+AP ANI Sbjct: 264 RAPADRIIIKDRIADSIFQQVLLRPEEYSVIATPNLNGDYLSDALAAQVGGLGMAPGANI 323 Query: 249 GDEHGLFEPVHGSAPDIAGKKIANPTATILSAVLMLRYLGEYEAADKVEKALEEVLALGL 308 GD + +FE HGSAP A NP++ ILS +ML YL EAA+ + + L + Sbjct: 324 GDRYAVFEATHGSAPKYANLDKINPSSLILSGTMMLEYLDWTEAANLIHEGLARTIQART 383 Query: 309 TTPDL 313 T DL Sbjct: 384 VTYDL 388 Lambda K H 0.318 0.138 0.390 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: 300 Number of extensions: 14 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: 333 Length of database: 416 Length adjustment: 30 Effective length of query: 303 Effective length of database: 386 Effective search space: 116958 Effective search space used: 116958 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: 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