Align phosphopentomutase (EC 5.4.2.7) (characterized)
to candidate 8499281 DvMF_0059 phosphoglucosamine mutase (RefSeq)
Query= BRENDA::Q6I7B6 (450 letters) >FitnessBrowser__Miya:8499281 Length = 450 Score = 171 bits (432), Expect = 6e-47 Identities = 140/465 (30%), Positives = 235/465 (50%), Gaps = 45/465 (9%) Query: 2 RLFGTAGIRGTL-WEKVTPELAMKVGMAVGTY-----KSGKALVGRDGRTSSVMLKNAMI 55 RLFGT G+RG + +T ++A+++G+A GT+ + + ++G+D R S + ++A+ Sbjct: 4 RLFGTDGLRGQVNIYPMTADVALRLGLAAGTHFRNGNRRHRVVIGKDTRLSGYVFESALT 63 Query: 56 SGLLSTGMEVLDADLIPTPALAWGTRKL-ADAGVMITASHNPPTDNGVKVFNGDGTEFYV 114 +GL + GM+V +PTPA+A+ TR + AD GV+I+ASHNP DNG+K F+ DG + Sbjct: 64 AGLCAAGMDVYLVGPLPTPAIAFLTRNMRADLGVVISASHNPFMDNGIKFFDKDGFKLPD 123 Query: 115 EQERGLEEIIFSGNFRKARWDEIKPVR-----NVEVIPDYINAVL--DFVGHET--NLKV 165 E E + +++ ++ +WD P R +E P L F H T ++V Sbjct: 124 EMENKITDMVLDPDW---QWDYPAPERVGRAAKIEDSPGRYIVYLKNSFPAHLTLDGMRV 180 Query: 166 LYDGANGAGSLVAPYLLREMGAKVLSVNAHVDGHFPGRKPEPRYENIAYLGKLVRELGVD 225 + D ANGA VAP L E+GA+V+ + +G + Y +A GK V E D Sbjct: 181 VLDCANGANYKVAPLALEELGAEVIKIGTEPNGLNINHQCGSLYPGVA-AGK-VLETRAD 238 Query: 226 LAIAQDGDADRIAVFDEKGNYVDEDTVIALFAKLYVEEHG--GGTVVVSIDTGSRIDAVV 283 + +A DGDADR+ V DEKG +D D ++AL A + T+V ++ + ++ + Sbjct: 239 VGLALDGDADRLIVVDEKGTVLDGDQIMALCADDMLRRGALRNNTLVATVMSNMALEVYM 298 Query: 284 ERAGGRVVRIPLGQPH--DGIKRYKAIFAAE-PWKLVHPKFGPWIDPFVTMGLLIKLIDE 340 + G +++R P+G + + ++R A E L+ G D + +++++ E Sbjct: 299 KERGCKLLRTPVGDRYVVEAMRREGANLGGEQSGHLIFMDHGTTGDGLMAALQILRIMRE 358 Query: 341 -NGPLSELVKEIPTYYLKKANVLCPDEYKAEVVRRAAEEVERKLSSE-IKEVLT-ISGFR 397 + PLSEL ++ + + NV VERK+ E + VL ++ Sbjct: 359 RDRPLSELAGQLQLFPQELINV----------------HVERKIPFEQCQPVLDGVAKVE 402 Query: 398 IALNDGSWILIRPSGTEPKIRVVAEAPTEKRRDELFEMAYSTVSR 442 L D +L+R SGTE RV+ E ++ L + TV + Sbjct: 403 AELGDRGRVLLRYSGTEAVCRVMVEGEDPEQVKRLASLLAETVQK 447 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: 489 Number of extensions: 30 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: 450 Length of database: 450 Length adjustment: 33 Effective length of query: 417 Effective length of database: 417 Effective search space: 173889 Effective search space used: 173889 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