Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate WP_007472804.1 CMTB2_RS00125 phosphoglycerate dehydrogenase
Query= reanno::Cola:Echvi_2777 (630 letters) >NCBI__GCF_000170735.1:WP_007472804.1 Length = 522 Score = 176 bits (445), Expect = 3e-48 Identities = 107/324 (33%), Positives = 182/324 (56%), Gaps = 16/324 (4%) Query: 233 INVLLLENVHPIGVEIMKQEGYNVEVV-SSAMSEEELCEKIKNVSIIGIRSKTQITKKVL 291 + ++ + +HP GVEI+K + ++EVV +S ++EL + I++ + RS T + +K L Sbjct: 1 MKAVICDPIHPAGVEILK-KAKDIEVVDASKTPKDELLKIIEDADGVITRSPTPVDEKFL 59 Query: 292 ENANRLMAVGAFCIGTNQIDLETCQEKGIAVFNAPFSNTRSVVELAISEIIFLMRNLHDK 351 +A +L A+ +G + +D+E C ++GI V N P +NT + VEL ++ ++ R+ + Sbjct: 60 SHAKKLKAIVRAGVGVDNVDIEACSKRGIVVMNIPTANTLAAVELTMAHLLTAARSFTNA 119 Query: 352 TLKM-HQGIWNKSASGSFEVRGKKLGIIGYGNIGAQLSVLAENMGMNVFYYDIVERLALG 410 + + WN+ E+ GKKLGIIG+GNIG+++ + A+ + M+V YD + Sbjct: 120 VWNLKKEHEWNREKWLGIELAGKKLGIIGFGNIGSRVGIRAKALEMDVIAYD--PYIDPS 177 Query: 411 NATKI-----DSLDELLETCDIISLHVDGRTENKNILNKEKIFKMKKGAILVNLSRGHVV 465 AT + DE+L+ CD I++H E N++ K++I KMK G +L+N +RG + Sbjct: 178 KATDLGCKYTTDFDEILK-CDFITIHTPKTPETINMITKKEIEKMKDGVVLINCARGGLY 236 Query: 466 DVPALRDALESGHLAGAAVDVFPTEPKNNDEPFESELIGCPNTILTPHIGGSTLEAQENI 525 + + + L+SG + +DVF EP FE E NT +TPHIG +T E+Q+ I Sbjct: 237 NENDVYEGLKSGKIRWLGIDVFEKEPVTEHPFFELE-----NTSVTPHIGANTKESQQRI 291 Query: 526 AQFVPGKIIEYINSGNTFNSVNFP 549 A IIE + + N++N P Sbjct: 292 AIQAAEAIIEALRGSSYPNALNLP 315 Score = 34.3 bits (77), Expect = 1e-05 Identities = 27/114 (23%), Positives = 47/114 (41%), Gaps = 9/114 (7%) Query: 520 EAQENIAQFVPGKII----EYINSGNTFNS----VNFPNIQLPFLKDAHRLIHIHQNAPG 571 E E V K++ EY SG + V F L F + + + PG Sbjct: 402 EKNETYKNLVQIKVLTDEGEYSISGTMLENHPRVVEFKGFDLEFEPKGKMIFFKNTDVPG 461 Query: 572 VLAKINQVLASYKINIVGQYLKTN-EKIGYVITDIDKRYSNDVIDALKEIEGTI 624 V+ ++ LA + INI L N E + +D + +V++ LK+++ + Sbjct: 462 VIGEVGMTLAKHNINIADFRLGRNKEGQAMAVIIVDNDVNEEVLNELKKLKAAL 515 Lambda K H 0.317 0.136 0.377 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: 754 Number of extensions: 45 Number of successful extensions: 5 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: 630 Length of database: 522 Length adjustment: 36 Effective length of query: 594 Effective length of database: 486 Effective search space: 288684 Effective search space used: 288684 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: 53 (25.0 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
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