Align phosphopentomutase (EC 5.4.2.7) (characterized)
to candidate BWI76_RS25130 BWI76_RS25130 phosphoglucosamine mutase
Query= BRENDA::Q6I7B6 (450 letters) >FitnessBrowser__Koxy:BWI76_RS25130 Length = 445 Score = 140 bits (353), Expect = 8e-38 Identities = 131/446 (29%), Positives = 216/446 (48%), Gaps = 33/446 (7%) Query: 2 RLFGTAGIRGTLWEK-VTPELAMKVGMAVGT----YKSGKALVGRDGRTSSVMLKNAMIS 56 + FGT GIRG + + +TPE +K+G A G + S K ++G+D R S ML++A+ + Sbjct: 5 KYFGTDGIRGRVGDAPITPEFVLKLGWAAGKVLARHGSRKIIIGKDTRISGYMLESALEA 64 Query: 57 GLLSTGMEVLDADLIPTPALAWGTRKL-ADAGVMITASHNPPTDNGVKVFNGDGTEFYVE 115 GL + G+ +PTPA+A+ TR A+AG++I+ASHNP DNG+K F+ +GT+ E Sbjct: 65 GLAAAGLSASFTGPMPTPAIAYLTRTFRAEAGIVISASHNPFYDNGIKFFSIEGTKLPDE 124 Query: 116 QERGLEEIIFSGNFRKARWDEIKPVRNVEVIPDYINAVLDFVGHE---TNLKVLYDGANG 172 E +E + + K R V+ YI +E +LKV+ D A+G Sbjct: 125 VEEAIEAEMEKELTCVDSAELGKASRIVDAAGRYIEFCKGTFPNELSLNSLKVVVDCAHG 184 Query: 173 AGSLVAPYLLREMGAKVLSVNAHVDGHFPGRKPEPRYENIAYLGKLVRELGVDLAIAQDG 232 A +AP + RE+GA+V+++ DG E ++ L V DL IA DG Sbjct: 185 ATYHIAPNVFRELGAQVIAMGCEPDG--LNINEEVGATDVRALQARVLAEKADLGIAYDG 242 Query: 233 DADRIAVFDEKGNYVDEDTVIALFAKLYVEE---HGGGTVVVSIDTGSRIDAVVERAGGR 289 D DR+ + D +GN VD D ++ + A+ + + GG + + G ++ +++ G Sbjct: 243 DGDRVIMVDHEGNKVDGDQILYIIAREGLRQGQLRGGAVGTLMSNMG--LELALKQLGIP 300 Query: 290 VVRIPLGQPHDGIKRYKAIFAAEPWKLVHPKFGPWIDPFVTMGLLIKLIDENGPLSEL-- 347 VR +G + K + W++ G I LL K +G ++ L Sbjct: 301 FVRAKVGDRYVLEK-----LQEKGWRIGAENSGHVI-------LLDKTTTGDGIVASLQV 348 Query: 348 VKEIPTYYLKKANVLCPDEYKAEVV--RRAAEEVERKLSSEIKEVLTISGFRIALNDGSW 405 V + +L ++ + +++ R E L E + +T + AL + Sbjct: 349 VAAMVRNHLSLHDLCSGMKMFPQLLVNVRFTEGSGNPLEHEHVKAVT-AEVEAALGNRGR 407 Query: 406 ILIRPSGTEPKIRVVAEAPTEKRRDE 431 +L+R SGTEP IRV+ E E++ E Sbjct: 408 VLLRKSGTEPLIRVMVEGEHEEQVHE 433 Lambda K H 0.318 0.138 0.402 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: 448 Number of extensions: 27 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 450 Length of database: 445 Length adjustment: 33 Effective length of query: 417 Effective length of database: 412 Effective search space: 171804 Effective search space used: 171804 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: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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