GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Shewanella loihica PV-4

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.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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