Align phosphoserine phosphatase (EC 3.1.3.3) (characterized)
to candidate Synpcc7942_0485 Synpcc7942_0485 phosphoglycerate mutase
Query= BRENDA::D3DFG8 (211 letters) >FitnessBrowser__SynE:Synpcc7942_0485 Length = 445 Score = 119 bits (299), Expect = 7e-32 Identities = 70/204 (34%), Positives = 114/204 (55%), Gaps = 5/204 (2%) Query: 2 VKLILVRHAESEWNPVGRYQGLLDPDLSERGKKQAKLLAQELSREHLDVIYSSPLKRTYL 61 V+L+LVRH E++WN R+QG +D L++ G+ QA+ A+ L+ +D SSP+ R Sbjct: 229 VRLLLVRHGETDWNRQKRFQGQIDIPLNDNGRAQARSAAEFLAPIQIDFAVSSPMARPKE 288 Query: 62 TALEIAEA-KNLEVIKEDRIIEIDHGMWSGMLVEEVMEKYPEDFRRWVEEPHKVEFQGGE 120 TA I E N E+ +DR+ EI HG+W G L EE+ ++ E + W ++P +V+ GE Sbjct: 289 TAELILERHPNCELSVDDRLQEIGHGLWEGKLEEEIAAEFGELLQLWKDQPEQVQMPEGE 348 Query: 121 SLASVYNR-VKGFLEEVRKRHWNQTVVVVSHTVPMRAMYCALLGVDLSKFWSFGCDNASY 179 +L V++R V + V T +VV+H + + C +LG+ + WS N + Sbjct: 349 NLQEVWDRSVAAWEAIVANAPEGSTGLVVAHDAVNKVILCHVLGLSPADIWSIKQGNGAV 408 Query: 180 SVIHMEER---RNVILKLNITCHL 200 +V+ +R R V+ +N+T HL Sbjct: 409 TVVDYPKRLDSRPVLQAMNLTLHL 432 Score = 101 bits (251), Expect = 2e-26 Identities = 67/215 (31%), Positives = 113/215 (52%), Gaps = 15/215 (6%) Query: 3 KLILVRHAESEWNPVGRYQGLLD-PDLSERGKKQAKLLAQELSREHLDVIYSSPLKRTYL 61 +++LVRH +S +N GR QG D L++RG A +A L+ Y SPL+R Sbjct: 4 RVVLVRHGQSSYNAAGRIQGRCDNSQLTDRGAADAVKVAAALNGIPFAAAYCSPLQRAKR 63 Query: 62 TALEIAEAKNLE--VIKEDRIIEIDHGMWSGMLVEEVMEKYPEDFRRWVEEPHKV----- 114 TA I E + D ++E+D +W G+ EEV +Y E +R+W E PH++ Sbjct: 64 TAEIIIEQIETPPALAVSDGLLEVDLPLWEGLSREEVRSQYAELYRQWHEAPHELVLTVP 123 Query: 115 EFQGGE----SLASVYNRVKGFLEEVRKRHWNQTVVVVSHTVPMRAMYCALLGVDLSKFW 170 + QGG + +++ + + F +++ +RH +QTV++V+H +R++ LGVD S + Sbjct: 124 DGQGGSREHAPVLALFEQARQFWKDLLERHRDQTVLLVAHNGILRSLIATALGVDPSAYQ 183 Query: 171 SFGCDNASYSVIHMEERRNVILK---LNITCHLGE 202 N SV++ + N + LN+T LG+ Sbjct: 184 VIRQSNCGISVLNFADGTNQPAQLECLNLTAPLGD 218 Lambda K H 0.320 0.136 0.408 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: 257 Number of extensions: 23 Number of successful extensions: 7 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: 211 Length of database: 445 Length adjustment: 27 Effective length of query: 184 Effective length of database: 418 Effective search space: 76912 Effective search space used: 76912 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 (21.8 bits) S2: 48 (23.1 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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