GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Phaeobacter inhibens BS107

Align L-lactaldehyde reductase (EC 1.1.1.77) (characterized)
to candidate GFF2678 PGA1_c27200 alcohol dehydrogenase, iron containing

Query= metacyc::STM4044-MONOMER
         (382 letters)



>FitnessBrowser__Phaeo:GFF2678
          Length = 381

 Score =  215 bits (548), Expect = 1e-60
 Identities = 127/374 (33%), Positives = 194/374 (51%), Gaps = 13/374 (3%)

Query: 14  GAGAIADMVNLVANKQWGKALIVTDGQLVKLGLLDSLFSALDEHQMSYHLFDEVFPNPTE 73
           GAG I ++    A     K L+VTD  L  L +  S    L+   +   +F EV PNP E
Sbjct: 16  GAGRIRELAEACATAGMKKPLLVTDKGLADLPVTQSTLDILEAAGLGRAMFCEVDPNPNE 75

Query: 74  ELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAYSGVGKV-----KNA 128
           + ++ G AAY++ + D +IAFGGGS +D  K V  +     P   +  +G        +A
Sbjct: 76  KNLEAGVAAYKAGDHDGVIAFGGGSGLDLGKMVAFMCGQNRPVWDFEDIGDWWTRADADA 135

Query: 129 GVPLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLEIPASVTA 188
             P++A+ TTAGT +E+   +VI DS    K++I  P ++P + + D  + + +P  +TA
Sbjct: 136 IAPIIAVPTTAGTGSEVGRASVITDSVTHQKKIIFHPKVLPTVVICDPELTVGMPKFITA 195

Query: 189 ATGMDALTHAVEAYVSVGAHPLTDANALEAIRLINLWLPKAVDDGHNLEAREQMAFGQYL 248
            TG+DA  H VEA+ S   HP++   ALE +RL+  +LP+A  DG ++EAR QM     +
Sbjct: 196 GTGLDAFAHCVEAFSSPHYHPMSQGIALEGMRLVKEYLPRAYADGTDIEARAQMMSAAAM 255

Query: 249 AGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFARIAQAMGV 308
              AF   GLG +HA++H  GA  N  HG  NA+ +  V  FN P    RF   A  +G+
Sbjct: 256 GATAFQK-GLGAIHAMSHPIGALFNTHHGTTNAVCMLAVLAFNAPEIADRFKTAADYLGI 314

Query: 309 ETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKALADPCAPCNPRT 368
                  +   +     ++ L+  +GIP G S+LGVT+  I   +  AL DP    NP  
Sbjct: 315 -------DGGFEGVCAYVQELNDSLGIPRGLSELGVTEAAIPELVKGALIDPSCGGNPVV 367

Query: 369 ASRDEVRGLYLEAL 382
             +  +  L+ +A+
Sbjct: 368 LDQANLTQLFKDAM 381


Lambda     K      H
   0.317    0.133    0.384 

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: 426
Number of extensions: 32
Number of successful extensions: 4
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: 382
Length of database: 381
Length adjustment: 30
Effective length of query: 352
Effective length of database: 351
Effective search space:   123552
Effective search space used:   123552
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 (21.7 bits)
S2: 50 (23.9 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