Align Aerobic glycerol-3-phosphate dehydrogenase; EC 1.1.5.3 (characterized)
to candidate WP_017558373.1 C892_RS0118455 glycerol-3-phosphate dehydrogenase/oxidase
Query= SwissProt::P18158 (555 letters) >NCBI__GCF_000341205.1:WP_017558373.1 Length = 522 Score = 200 bits (508), Expect = 1e-55 Identities = 154/494 (31%), Positives = 248/494 (50%), Gaps = 49/494 (9%) Query: 24 DLFIIGGGITGAGTALDAASRGMKVALSEMQDFAAGTSSRSTKLVHGGLRYLKQFEVKMV 83 DL ++G G+TGAGTALDAA+RG++VAL + D A GTS S+KLVHGGLRYL + ++ + Sbjct: 34 DLLVVGAGVTGAGTALDAAARGLRVALVDRGDLAHGTSRWSSKLVHGGLRYLAKGQIGVA 93 Query: 84 AEVGKERAIVYE-NGPHVTTPEWMLLPFHKG-GTFGSFTTSIGLRVYDFLAGVKKSERRS 141 E +ER ++ E PH+ M++P H+G T + G+ V D L ++RR+ Sbjct: 94 VESARERGVLMETTAPHLVRALPMVIPLHEGVDTAHAAAARAGMAVGDVLRAAAGTDRRA 153 Query: 142 M-----LSAKETLQKEPLVKKDGLKGGGYYVEYR-TDDARLTIEVMKEAVKFGAEPVNYS 195 + L+ ++TL+ P V+++GL+GG + + TDDARL + + + A GA V Sbjct: 154 LPRSRRLTVEQTLRLLPGVRREGLRGGLLSFDGQLTDDARLVVALARTAAGLGAGVVTRC 213 Query: 196 KVKELLYEKGKAVGVLIEDVLTKKEYKVYAKKIVNATGPWVDQLREKDHSKNGKHLQHTK 255 + L G ++ D+ T + +V A+ +VNATG + +L + L+ ++ Sbjct: 214 AAERL-----GGDGAVLRDLRTGRRIEVAARAVVNATGVYAGELVPQ------VRLRPSR 262 Query: 256 GIHLVF-DQSVFPLKQAVYFDTPD--GRMVFAIPR-EGKTYVGTTDTVYKEAL-EHPRMT 310 G H V +SV K A+ P R VFA+P+ +G+ + G TD L E P+ Sbjct: 263 GTHAVLRAESVGRPKAALMVPVPGTANRFVFALPQPDGRVFAGLTDEPVDGPLPEVPQAP 322 Query: 311 TEDRDYVIKSINYMFPELNITANDIESSWAGLRPLIHEEGKDPSEISRKDEIWTSDSGLI 370 D D++++ +N + D+ ++AGLRPL+ G +++SR + S G++ Sbjct: 323 EGDVDFLLEVLNRALGTA-LGRADVAGAYAGLRPLLEGRGGTSADLSRSHAVIRSAEGVL 381 Query: 371 TIAGGKLTGYRKMAEHIVDLVRDRLKEEGEKDFGPCKTKNMPISGGHVGGSKNLMSFVTA 430 T+ GGKLT YR+MAE VD G C+T+ +P+ G + ++ V A Sbjct: 382 TVVGGKLTTYRRMAEEAVDAAVGAAGLAA----GACRTRALPLVG---AAPRAVLDAVDA 434 Query: 431 KTKEGIAAGLSEKDAKQLAIRYGSNVDRVFDRVEALKDEAAKRNIPVHIL-AEAEYSIEE 489 +++ RYG+ V A D R + + AE +++E Sbjct: 435 --------------PRRMIARYGTEAPAVV--AAAGGDPEMLRPVAAGVTPAEMRFAVEA 478 Query: 490 EMTATPADFFVRRT 503 E D RRT Sbjct: 479 EGALDAEDVLDRRT 492 Lambda K H 0.316 0.134 0.386 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: 580 Number of extensions: 20 Number of successful extensions: 5 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: 555 Length of database: 522 Length adjustment: 35 Effective length of query: 520 Effective length of database: 487 Effective search space: 253240 Effective search space used: 253240 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 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