Align Probable methanogen homoaconitase large subunit; HACN; EC 4.2.1.114; Homoaconitate hydratase (uncharacterized)
to candidate 6936140 Sama_0337 isopropylmalate isomerase large subunit (RefSeq)
Query= curated2:Q8TLF1 (424 letters) >FitnessBrowser__SB2B:6936140 Length = 470 Score = 246 bits (627), Expect = 1e-69 Identities = 163/462 (35%), Positives = 231/462 (50%), Gaps = 55/462 (11%) Query: 14 TISEKIFSRAAGTEAKANDFVLADVDYAMAHDGTSVLAVNAFKEMEMEKVWDPSRIVVPF 73 T+ EK++ E A + + VD + H+ TS A + K M + + Sbjct: 4 TLYEKVWDAHLVVEP-AGEAPIIYVDRHLVHEVTSPQAFSGLK-MAGRPLRAVEKTFATM 61 Query: 74 DHIAPANNETSATLQREIREWVKEQG---------IPNFYEVGEGICHQVLPENGFALPG 124 DH + + L R V+ + + + +GI H + PE G LPG Sbjct: 62 DHNTSTKSASLTALSPMARTQVETLADNCRDFNVRLYDIHHPNQGIVHVMGPELGITLPG 121 Query: 125 KLVVGADSHSCTYGAFGAFATGVGATDMAEIFATGKLWFKVPESFRMTVEGSLRKGVYAK 184 ++V DSH+ T+GAFGA A G+G +++ + AT L ++ ++ V G + G+ AK Sbjct: 122 TVIVCGDSHTATHGAFGALAFGIGTSEVEHVLATQTLRQLKAKTMKIEVRGKVADGITAK 181 Query: 185 DLTLYLIGKTGIAGATYKAVEFYGQAIRELTVAGRMTLCNMAIEMGAKTGIVPPDEKTFE 244 D+ L +IGK G+ G T VEF G+AIR+L++ GRMTLCNMAIEMGAK G+V PDE TF Sbjct: 182 DIVLAIIGKIGMDGGTGYVVEFCGEAIRDLSMEGRMTLCNMAIEMGAKAGMVAPDETTFA 241 Query: 245 FLKNR-----------AAATYEPVYADPDAVYLEEFTYDADDIEPQV------------- 280 +L+ R A A + ++ D DAV+ E +A I PQ+ Sbjct: 242 YLEGREFAPKGDAWQQALADWRELHTDADAVFDAEVVLEAAAIAPQLTWGTNPGQVVAID 301 Query: 281 -ACPHQVDNVKPVGEVE------------GT-----HVDQVFIGTCTNGRLEDLEVAAAV 322 P+ D PV GT +++VFIG+CTN R+EDL AAA Sbjct: 302 GVVPNPADETNPVVRTSMEKALAYVDLTPGTPMTDIAINKVFIGSCTNSRIEDLRAAAAQ 361 Query: 323 LKGKQVA--VRTIVIPASRTTLLAAIENGTMETLLKAGVTLATPGCGPCLGAHQGVLGEG 380 KG++VA V IV+P S L A G + L+AG PGC CL + L G Sbjct: 362 AKGRKVASGVTAIVVPGSGQVKLQAEAEGLDKIFLEAGFEWRLPGCSMCLAMNDDRLEAG 421 Query: 381 EVCVSTANRNFKGRMGKGGFIYLASPATAAASALTGEITDPR 422 + C ST+NRNF+GR G+G +L SPA AAA+A+ G D R Sbjct: 422 DRCASTSNRNFEGRQGRGSRTHLVSPAMAAAAAVAGHFVDIR 463 Lambda K H 0.318 0.135 0.400 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: 486 Number of extensions: 25 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: 424 Length of database: 470 Length adjustment: 33 Effective length of query: 391 Effective length of database: 437 Effective search space: 170867 Effective search space used: 170867 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 Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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