Align glycerol-3-phosphate dehydrogenase; EC 1.1.5.3 (characterized)
to candidate AO353_04190 AO353_04190 glycerol-3-phosphate dehydrogenase
Query= CharProtDB::CH_091834 (512 letters) >FitnessBrowser__pseudo3_N2E3:AO353_04190 Length = 512 Score = 783 bits (2021), Expect = 0.0 Identities = 378/512 (73%), Positives = 438/512 (85%) Query: 1 MSQAHTPSAPLAEVYDVAVVGGGINGVGIAADAAGRGLSVFLCEQHDLAQHTSSASSKLI 60 M + P PLAEVYD+AV+GGGINGVGIAADAAGRGLSVFLCE+ DLA HTSSASSKLI Sbjct: 1 MPTSTLPMPPLAEVYDIAVIGGGINGVGIAADAAGRGLSVFLCEKDDLASHTSSASSKLI 60 Query: 61 HGGLRYLEHYEFRLVREALAEREVLLAKAPHIVKPLRFVLPHRPHLRPAWMIRAGLFLYD 120 HGGLRYLEHYEFRLVREALAEREVLLAKAPHIVKP+RFVLPHRPHLRPAWMIRAGLFLYD Sbjct: 61 HGGLRYLEHYEFRLVREALAEREVLLAKAPHIVKPMRFVLPHRPHLRPAWMIRAGLFLYD 120 Query: 121 HLGKREKLPASRGLRFTGSSPLKAEIRRGFEYSDCAVDDARLVVLNAISAREHGAHVHTR 180 HLGKREKL S+ L+F S LK+EI +GFEYSDC VDDARLVVLNA++ARE GAHVHT+ Sbjct: 121 HLGKREKLAGSKSLKFGADSALKSEITKGFEYSDCWVDDARLVVLNAMAAREKGAHVHTQ 180 Query: 181 TRCVSARRSKGLWHLHLERSDGSLYSIRARALVNAAGPWVARFIQDDLKQKSPYGIRLIQ 240 TRCVSARRSKGLW L+LER+DG L+SIRA+ALVNAAGPWVA+FI+DDLK +SPYGIRLIQ Sbjct: 181 TRCVSARRSKGLWELNLERTDGRLFSIRAKALVNAAGPWVAKFIRDDLKMESPYGIRLIQ 240 Query: 241 GSHIIVPKLYEGEHAYILQNEDRRIVFAIPYLDRFTMIGTTDREYQGDPAKVAISEEETA 300 GSH+IVPKLYEGEHA+ILQNED+RIVF IPYL++FT+IGTTDREY GDPAKV I+E ET Sbjct: 241 GSHLIVPKLYEGEHAHILQNEDQRIVFTIPYLNQFTLIGTTDREYTGDPAKVTITEGETD 300 Query: 301 YLLQVVNAHFKQQLAAADILHSFAGVRPLCDDESDEPSAITRDYTLSLSAGNGEPPLLSV 360 YLL+VVNAHFK+Q++ +DILH+++GVRPLC+DESD PSA+TRDYTL+LS E PLLSV Sbjct: 301 YLLKVVNAHFKKQISRSDILHTYSGVRPLCNDESDNPSAVTRDYTLALSGSAEEAPLLSV 360 Query: 361 FGGKLTTYRKLAESALTQLQPFFANLGPAWTAKAPLPGGEQMQSVEALTEQLANRYAWLD 420 FGGKLTTYRKLAESA+ QL P+F + P+WTA+A LPGGE M + +AL+ + +++ WL Sbjct: 361 FGGKLTTYRKLAESAMAQLAPYFKGMKPSWTAQATLPGGEDMTTPQALSALIRDKFDWLP 420 Query: 421 RELALRWARTYGTRVWRLLDGVNGEADLGEHLGGGLYAREVDYLCKHEWAQDAEDILWRR 480 E+A RWA TYG+R WRLL+GV D+GEHLGGGLY REVDYLC EWA A DILWRR Sbjct: 421 TEIARRWATTYGSRTWRLLEGVQSLKDMGEHLGGGLYTREVDYLCSEEWATSAHDILWRR 480 Query: 481 SKLGLFLSPSQQVRLGQYLQSEHPHRPRVHAA 512 SKLGLF + ++Q + YL +R ++ AA Sbjct: 481 SKLGLFTTQAEQENVQLYLNKLEQNRSKIEAA 512 Lambda K H 0.321 0.136 0.415 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: 882 Number of extensions: 29 Number of successful extensions: 1 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: 512 Length of database: 512 Length adjustment: 35 Effective length of query: 477 Effective length of database: 477 Effective search space: 227529 Effective search space used: 227529 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: 52 (24.6 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:
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