Align UDP-glucose-hexose-1-phosphate uridylyltransferase (EC 2.7.7.12) (characterized)
to candidate 5209835 Shew_2288 galactose-1-phosphate uridylyltransferase (RefSeq)
Query= BRENDA::P09148 (348 letters) >FitnessBrowser__PV4:5209835 Length = 363 Score = 437 bits (1125), Expect = e-127 Identities = 200/345 (57%), Positives = 253/345 (73%), Gaps = 1/345 (0%) Query: 2 TQFNPVDHPHRRYNPLTGQWILVSPHRAKRPWQGAQETPAKQVLPAHDPDCFLCAGNVRV 61 +QF+ +HPHRR+NPLTG+W+L+SPHR+KRPWQG E P++D +CFLC GN R+ Sbjct: 9 SQFSTDEHPHRRFNPLTGEWVLLSPHRSKRPWQGQTEALDLTTAPSYDSECFLCPGNKRI 68 Query: 62 TGDKNPDYTGTYVFTNDFAALMSDTPDAPESHDPLMRCQSARGTSRVICFSPDHSKTLPE 121 G++NP Y T+VF NDFAAL SD P A + DPL R ++ G SRV+CFSPDHS TL + Sbjct: 69 NGEQNPKYDTTFVFQNDFAALNSDGPKA-QGEDPLFRFETVEGESRVLCFSPDHSLTLAQ 127 Query: 122 LSVAALTEIVKTWQEQTAELGKTYPWVQVFENKGAAMGCSNPHPHGQIWANSFLPNEAER 181 L A+ ++ WQ Q+ LGK Y WVQVFENKGAAMGCSNPHPHGQIWA++ LP Sbjct: 128 LDPEAMQAVIAAWQSQSELLGKKYLWVQVFENKGAAMGCSNPHPHGQIWAHNHLPTLVAT 187 Query: 182 EDRLQKEYFAEQKSPMLVDYVQRELADGSRTVVETEHWLAVVPYWAAWPFETLLLPKAHV 241 + + +Y+ + S +L DYV+REL R VV W+A+VPYWA+WPFETL+LP+ + Sbjct: 188 KQQRLADYYQQHHSNLLGDYVERELQQEVRIVVSNHDWVALVPYWASWPFETLVLPRFDI 247 Query: 242 LRITDLTDAQRSDLALALKKLTSRYDNLFQCSFPYSMGWHGAPFNGEENQHWQLHAHFYP 301 R+T+LT R L + LT RYDNLFQC+FPYSMGWHGAPF+G+++ W LHAHFYP Sbjct: 248 RRMTELTAETRESLGEIIGALTVRYDNLFQCAFPYSMGWHGAPFDGQDHPEWCLHAHFYP 307 Query: 302 PLLRSATVRKFMVGYEMLAETQRDLTAEQAAERLRAVSDIHFRES 346 PLLRSA+V+KFMVGYE+LAE QRD+T EQAA RLR S IH++ S Sbjct: 308 PLLRSASVKKFMVGYELLAEIQRDITPEQAAARLREQSPIHYKSS 352 Lambda K H 0.319 0.133 0.425 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: 505 Number of extensions: 16 Number of successful extensions: 2 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: 348 Length of database: 363 Length adjustment: 29 Effective length of query: 319 Effective length of database: 334 Effective search space: 106546 Effective search space used: 106546 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: 49 (23.5 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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