Align fused D-3-phosphoglycerate dehydrogenase / phosphoserine phosphatase (EC 1.1.1.95; EC 3.1.3.3) (characterized)
to candidate CA265_RS22635 CA265_RS22635 phosphoserine phosphatase
Query= reanno::Cola:Echvi_2777 (630 letters) >FitnessBrowser__Pedo557:CA265_RS22635 Length = 433 Score = 301 bits (772), Expect = 3e-86 Identities = 151/327 (46%), Positives = 225/327 (68%), Gaps = 5/327 (1%) Query: 7 FIIDFDSTFTQVEALDILGEISLRNDPKRDEKLQAIKDITDLGMEGKLNLRESLERRIEI 66 +IIDFDSTFTQVEALD L ISL+N P ++ Q I+D T+ MEGKL+ ESL +R+++ Sbjct: 8 YIIDFDSTFTQVEALDELARISLKNHPDKEAIFQKIEDYTNFAMEGKLSFSESLAQRVKL 67 Query: 67 LQANKSQIAELIDALKQKVSKSFQRNREFFQENAENIYILSNGFKDFITPVVAAYGLKEE 126 L+AN+ + +LI LK+KVS SF RN EFF+++A+ + I+S GFK+FITPVV+ Y +K+E Sbjct: 68 LEANEDHLKQLIKHLKKKVSTSFSRNAEFFKKHADEVLIVSGGFKEFITPVVSQYHIKKE 127 Query: 127 NVFANDFIYDEAGNIIDLNKENLLSNNNGKPATIKSLKLEGDVYVIGDGYTDYEIKASGL 186 N++AN F+ G IID + N LS GK ++ LKLEG+++ IGDGY+D++++ SG+ Sbjct: 128 NIYANTFVTTGDGKIIDYDHANPLSEEGGKVKLLQHLKLEGELFGIGDGYSDFQLRESGI 187 Query: 187 ANKFYAFTENINRPKVSSKADHIAPSLDEILYVNKMNKKFSYPKSRINVLLLENVHPIGV 246 NKF+AFTENI R + SKADH+ PS DE LYVN + + SYPK+RI L++ +V P+ + Sbjct: 188 INKFFAFTENIARESIVSKADHVTPSFDEFLYVNDLPRAISYPKNRILCLVIGDVDPLTI 247 Query: 247 EIMKQEGYNVEVVSSAMSEEELCEKIKNVSIIGIRSKTQITKKVLENANRLMAVGAFCIG 306 I+K +G ++ +S + +K+V II + +I K+ L+NA +L +G Sbjct: 248 AILKNDGLSIRHKTSFED-----KYVKDVGIILLADGEKINKEQLKNAAKLKTIGYLGNA 302 Query: 307 TNQIDLETCQEKGIAVFNAPFSNTRSV 333 N+IDL+ C ++GI VF+ P +N R++ Sbjct: 303 KNKIDLDLCTKQGIVVFDDPKNNPRNI 329 Score = 125 bits (315), Expect = 3e-33 Identities = 55/103 (53%), Positives = 79/103 (76%) Query: 528 FVPGKIIEYINSGNTFNSVNFPNIQLPFLKDAHRLIHIHQNAPGVLAKINQVLASYKINI 587 F+P ++ +++N+G T+ S NFPN+QLP ++ +HRLIHIH+N PG++AKIN V A + INI Sbjct: 331 FIPKRVADFMNTGATYLSSNFPNLQLPKIEKSHRLIHIHKNVPGIMAKINTVFAKHDINI 390 Query: 588 VGQYLKTNEKIGYVITDIDKRYSNDVIDALKEIEGTIRFRILY 630 V Q+L TN +IGY ITDI+ Y + +LK+IE TI+FR+LY Sbjct: 391 VSQFLMTNPEIGYAITDINAEYDKQLFKSLKKIEHTIKFRVLY 433 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: 741 Number of extensions: 33 Number of successful extensions: 3 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: 433 Length adjustment: 35 Effective length of query: 595 Effective length of database: 398 Effective search space: 236810 Effective search space used: 236810 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: 52 (24.6 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