Align Phosphomannomutase/phosphoglucomutase; PMM / PGM; EC 5.4.2.2; EC 5.4.2.8 (uncharacterized)
to candidate GFF2403 PGA1_c24340 phosphomannomutase/phosphoglucomutase AlgC
Query= curated2:Q88C93 (463 letters) >FitnessBrowser__Phaeo:GFF2403 Length = 498 Score = 224 bits (571), Expect = 5e-63 Identities = 152/452 (33%), Positives = 240/452 (53%), Gaps = 21/452 (4%) Query: 14 FRAYDIRGVVGKTLHAETAYWIGRAIGAQSLAQGEPQV-SVGRDGRLSGPMLVEQLIKGL 72 FR YD R + ++ +G +G Q +G P V +V D R + LI GL Sbjct: 26 FREYDARWKYPEEINLPGMTALGLGLGTQMHKRGIPPVIAVANDYRDYSVAIKHALIIGL 85 Query: 73 VDAGCNVSDVGLVPTPALYYAANVLAGKSGVMLTGSHNPSDYNGFKIVIAGDTLANEQIQ 132 + AG V D+G +P Y+A L + M+T SHNP+ + G K+ Sbjct: 86 MQAGIEVRDIGPALSPMAYFAQFHLDVPAVAMVTASHNPNGWTGVKMGFERPLTHGPDEM 145 Query: 133 ALLTRLKTNDLTLAQ--GRVEKVE-ILDRYFKQIVGDVKLAKKLKVVVDCGNGAAGVVAP 189 L + N +A+ G + V+ + + Y +VGD K+++ LKVV GNG A AP Sbjct: 146 GELRDIVLNGEGVARPGGSYQFVDGVKEAYLDDLVGDFKMSRPLKVVCATGNGTASAFAP 205 Query: 190 QLIEALGCEVIPLFCEVDGNFPNHHPDPGKPENLEDLIAKVKETGADIGLAFDGDGDRVG 249 +L E +G EV+ +D FP+++P+P E L D+ A VK +GAD+ L FDGDGDR G Sbjct: 206 ELFERMGVEVVDSHNALDYTFPHYNPNPEAMEMLHDMSASVKASGADMALGFDGDGDRCG 265 Query: 250 VVTNTGSIVYPDRLLMLFAQDVLSRNPGAEIIFDVKCTRRLT--PLIEQHGGRALMWKTG 307 VV + G ++ D++ ++ A+D+ P + + DVK T P ++ +G A WKTG Sbjct: 266 VVDDEGEEIFADKVGVIMARDLSKLYPNSTFVADVKSTGLFASDPELKANGVTADYWKTG 325 Query: 308 HSLIKKKMKQTGSLLAGEMSGHIFIKER-WYGFDDGIYSAARLLEILSKT-EQSAENLFA 365 HS +K+++K+ G+L E SGH F+ E G+D G+ A + +++ + ++S +L Sbjct: 326 HSHMKRRVKEIGALAGFEKSGHYFLAEPVGRGYDCGMRVAVEICKLMDRNPDKSMSDLRK 385 Query: 366 AFPNDISTPEINIDVTDEGKFSIID----ALQRDADWGEA-------NLTTIDGVRVDYA 414 A P +TP ++ D K+++++ L A+ GE + T++G RV Sbjct: 386 ALPKTWATPTMSPYCADTEKYTVLERLVAKLVAKAEAGETLADRPIKEVVTVNGARVILD 445 Query: 415 NG-WGLVRASNTTPVLVLRFE-ADSDAELQRI 444 NG WGLVRAS+ TP LV+ E ++S+AEL+ I Sbjct: 446 NGSWGLVRASSNTPNLVVVCESSESEAELREI 477 Lambda K H 0.319 0.138 0.406 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: 575 Number of extensions: 39 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: 463 Length of database: 498 Length adjustment: 34 Effective length of query: 429 Effective length of database: 464 Effective search space: 199056 Effective search space used: 199056 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 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 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