Align Bifunctional phosphoglucose/phosphomannose isomerase; Glucose-6-phosphate isomerase; GPI; EC 5.3.1.9; Mannose-6-phosphate isomerase; EC 5.3.1.8; Phosphoglucose isomerase; PGI; Phosphomannose isomerase; PMI (uncharacterized)
to candidate WP_010936286.1 DET_RS02725 bifunctional phosphoglucose/phosphomannose isomerase
Query= curated2:Q44407 (339 letters) >NCBI__GCF_000011905.1:WP_010936286.1 Length = 355 Score = 207 bits (527), Expect = 3e-58 Identities = 123/336 (36%), Positives = 186/336 (55%), Gaps = 1/336 (0%) Query: 1 MFESVYNLPEQIQKAYEIGKNISVNVKAEDIDKVVITGLGGSAIGGNLLRVFVLDKCKIP 60 M + + +P ++A+E + +++ + +VVI G+G S + L V D+CKIP Sbjct: 20 MLDELRRMPSLCKQAWETAEALNLPEDYRAVKQVVILGMGTSGVAAQLAERIVRDECKIP 79 Query: 61 VIVNRDYVLPAYVDSKTLVIASSYSGNTEETLSAYQDAKAKGAKIIAITTGGKLKEFAEK 120 + +++DY+LPAYV + TLVIASS SG+TEE +S + A ++ AK++ +TTGG+LKE A Sbjct: 80 IYLHQDYLLPAYVSADTLVIASSSSGSTEEVVSCFNQAASRQAKLLVLTTGGELKEMAAG 139 Query: 121 DGFDVITIPSGLQPRAALGYSFIPLLMLFVKLGLIEPVDDQIEETVKVLSDLRERYKPEV 180 + +P A+ Y +P+L + KLG I ++ E++ VLS + ER + Sbjct: 140 HNIPGLVYDYTYRPSTAIAYGVLPVLSILHKLGFIPNKSAEVSESLIVLSQIAERLSEKY 199 Query: 181 PEEKNLAKRLTLKLWNKLPIIYGISGTTEVIAERWKGQICENSKSPAYFNVFSELNHNEI 240 N AK+L KL + + +G SG T A R+K Q+ EN+K A+ E+NHN + Sbjct: 200 QTSNNPAKQLADKLEGRAVMAFG-SGVTFPAARRFKTQLNENAKCFAFAEEIPEMNHNSV 258 Query: 241 VGTESPKHILGLFEIVMLHDTEDHKRNAIRMDITKDLIKGVVSGVNDIYSIGNSRLARMF 300 VG + P++ + VM T KR RM IT D++ V I G S L + Sbjct: 259 VGYQLPQNSGRYWAAVMFKTTFLSKRIHQRMKITTDILHQAKIPVFSIDGYGFSPLCQAL 318 Query: 301 SLIYLGDYVSLYLATLYQNDPTPVKKIDILKNKLAE 336 SLI GD+VSLYLA L DP P+ +D K +LAE Sbjct: 319 SLILQGDFVSLYLAFLNGVDPYPIDAVDYFKQELAE 354 Lambda K H 0.317 0.138 0.387 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: 271 Number of extensions: 8 Number of successful extensions: 2 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: 339 Length of database: 355 Length adjustment: 29 Effective length of query: 310 Effective length of database: 326 Effective search space: 101060 Effective search space used: 101060 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 (21.6 bits) S2: 49 (23.5 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 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:
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