Align Glycerol kinase; EC 2.7.1.30; ATP:glycerol 3-phosphotransferase; Glycerokinase; GK (uncharacterized)
to candidate WP_013403936.1 CALHY_RS10535 xylulokinase
Query= curated2:Q662C3 (501 letters) >NCBI__GCF_000166355.1:WP_013403936.1 Length = 502 Score = 194 bits (493), Expect = 6e-54 Identities = 152/481 (31%), Positives = 238/481 (49%), Gaps = 48/481 (9%) Query: 3 YILSIDQGTTSSRAIVFDKHANIKGLAQKEFTQIYPQPSWVEHDPTEIWGSQLGVITEAL 62 Y + ID GT+ ++ I+ D NI A E+ PQ W E +P + W + + I L Sbjct: 2 YFIGIDVGTSGTKTILTDSKGNILATATFEYPLYQPQIGWAEQNPEDWWDASVKGIKAVL 61 Query: 63 ANSRILPNEVDAIGITNQRETTVIWEKSTGKPIYNAIVWQDRRTAKICDQLT-KEGKDKI 121 S++ P EV A+G+T Q V+ +K+ I +I+W D+RTAK CD++T K GK+++ Sbjct: 62 EKSKVDPKEVKAVGLTGQMHGLVMLDKNY-NVIRPSIIWCDQRTAKECDEITEKIGKERL 120 Query: 122 ILEKTGLVLDSYFSGTKILWILDNVEGARQKAENGELCFGTI--DTWLLWNLTQKKVHAT 179 I E T + F+ +KILW+ +N + +N E + + ++ + LT + AT Sbjct: 121 I-EITANPALTGFTASKILWVRNN------EPQNYEKVYKILLPKDYIRFKLTGE--FAT 171 Query: 180 DYSNASRTLLLNIKTLEWDDELLKILNIPKAILPELKESSTIYGETDK------SIFGAE 233 D S+AS LL+IK W DE+L+ L I K +L ++ ES + G+ + ++ Sbjct: 172 DVSDASGMQLLDIKNRCWSDEVLEKLEIDKDLLGKVYESPEVTGKVSRQASEITGLWEGT 231 Query: 234 IPIAGIAGDQFAATFGQACLKKGMAKNTYGTGCFLTVNIGKEPIINHERLLTSI-AWGRK 292 + +AG GDQ A G +K G+ +T G+ + ++ + I R+ T A K Sbjct: 232 LVVAG-GGDQAAGAVGNGIVKTGVISSTIGSSGVVFAHLDEFKIDPQGRVHTFCHAVPGK 290 Query: 293 KTVTYVLEGSVFIGGAVIQWLRDGLEFFRKSS------------DAES-LASSASDNGGV 339 V V +G+ G ++W RD K++ D E+ LA+ SD G+ Sbjct: 291 WHVMGVTQGA----GLSLKWFRDNFAHIEKAAFEFIDKDPYILMDQEAELANPGSD--GL 344 Query: 340 YFVPAFVGLGAPHWDSYARGTIIGITRGSTKAHITRAALESIAF---QSFDILNTMKKSI 396 F+P +G P D YA+G GIT T+ RA +E + F DIL+ M Sbjct: 345 VFLPYLMGERTPILDPYAKGIFFGITAKHTRREFIRAVMEGVVFSLKNCLDILHEM---- 400 Query: 397 PNFEIKELRVDGGASQNNLLMQFQADLLECKVVRPKITETTALGAAYLAGLASGYWQSAE 456 E+KE+RV GG +++ L Q QAD+ E V E A GAA LA + +G + E Sbjct: 401 -GIEVKEVRVSGGGAKSKLWRQMQADIFEMDVWTLNSKEGPAFGAAILATVGAGVYNKVE 459 Query: 457 E 457 E Sbjct: 460 E 460 Lambda K H 0.317 0.133 0.397 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: 586 Number of extensions: 29 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: 501 Length of database: 502 Length adjustment: 34 Effective length of query: 467 Effective length of database: 468 Effective search space: 218556 Effective search space used: 218556 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