Align Glycerol-3-phosphate dehydrogenase; EC 1.1.5.3 (characterized, see rationale)
to candidate WP_043769224.1 U743_RS14550 glycerol-3-phosphate dehydrogenase/oxidase
Query= uniprot:Q92LM5 (503 letters) >NCBI__GCF_000733765.1:WP_043769224.1 Length = 514 Score = 217 bits (553), Expect = 7e-61 Identities = 178/491 (36%), Positives = 238/491 (48%), Gaps = 30/491 (6%) Query: 7 FDVFVIGGGINGCGIARDAAGRGYSVALAEMSDFASGTSSGSTKLIHGGLRYLEHYEFRL 66 FDV V+GGGI G A DAA RG AL + D+ +GTSS S+KLIHGGLRYLE++E L Sbjct: 21 FDVLVVGGGIYGAWAAYDAASRGLRTALIDAEDWGAGTSSASSKLIHGGLRYLENFELGL 80 Query: 67 VREALMEREVLWAMAPHVIWPMRFVLPFHKGGPRPAWLIRLGLFLYDHIG-GRKLLPATK 125 VR AL ER VL +APH++ P+ FVLP +G +R GL LYD + GR+ + K Sbjct: 81 VRHALTERRVLARLAPHMVRPINFVLPVWQGARVGMARLRAGLMLYDTLAWGRQPVQRHK 140 Query: 126 TLD----MTRDP--AGAPLKGLFTKAFEYSDGWVDDARLVVLNARDAADRGARIMARTRV 179 + + R P A A L+G F Y D DDARLV L A GA R Sbjct: 141 RFNRERLLRRYPFLADAGLRG----GFRYGDCQEDDARLVTLVVAAAQAAGAVCANHVRA 196 Query: 180 VSARRE--GGRWAIEIESTETGARETMRARMLVNAAGPWVDRVLSEAVGNNDVRNVRLVQ 237 + +R+ G + T AR T+ A V GPWV+ E G V+ V+ Sbjct: 197 EALQRDNTGTVTGATLRDTLGDARWTLHAGHTVGTVGPWVE----ELTGAQSPA-VQFVK 251 Query: 238 GSHIVVKKKFDDPRAYFFQNP-DGRIMFAIPYQDEFTLIGTTDRDFTGNPADVRISDAEI 296 G+H+V+ D A+ P DGR+ F IPY + TL+GTT+ PAD R SD E Sbjct: 252 GTHLVMSGIPDCHSAFLLNAPQDGRVFFVIPYYNR-TLVGTTEVSVNA-PADARPSDEEC 309 Query: 297 DYLCRAASEYFSD-PVGREDIVWTYSAVRPLFDDGASKAQEATRDYVLRVENGDAPLLNV 355 YL AA + P EDI+ ++ +R L GA + +R++ + AP L V Sbjct: 310 RYLLAAAHAWMPGLPWREEDIIQRFAGIRTLAAQGAGSLSKVSREFEI---TQPAPGLTV 366 Query: 356 -FGGKLTTYRRLAESALEKIGETIGEKGRKWTAVSHLPGGDFPAAGYDD--EVAKLRTRY 412 GGK TT R A ++ + +G K + T + LPG D E A+ R Sbjct: 367 PVGGKYTTARLDAAEIIDSVCGHLGVKAKSVTDRAPLPGAPPADNSLGDWLEDAQRRLCA 426 Query: 413 PFLTASHARRLVRLYGTRAAQLLGNAASEADLGKHFGADLYAAEVDWLIV--QEWALRAE 470 L + A + +GTR L ++ L D A V+ + E A+ AE Sbjct: 427 LGLDEAAAMQAALRHGTRVDTLCARLEADKGLATRIRPDCPFARVEAAVAISDEMAMTAE 486 Query: 471 DVLWRRTKLGL 481 DVL RR L L Sbjct: 487 DVLRRRLPLDL 497 Lambda K H 0.321 0.137 0.417 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: 632 Number of extensions: 34 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: 503 Length of database: 514 Length adjustment: 34 Effective length of query: 469 Effective length of database: 480 Effective search space: 225120 Effective search space used: 225120 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 (21.9 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 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