GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Thermodesulforhabdus norvegica DSM 9990

Align L-lactaldehyde reductase (EC 1.1.1.77) (characterized)
to candidate WP_093396475.1 BM091_RS13300 L-threonine dehydrogenase

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



>NCBI__GCF_900114975.1:WP_093396475.1
          Length = 388

 Score =  328 bits (840), Expect = 2e-94
 Identities = 179/377 (47%), Positives = 242/377 (64%), Gaps = 1/377 (0%)

Query: 7   LPKISLHGAGAIADMVNLVANKQWGKALIVTDGQLVKLGLLDSLFSALDEHQ-MSYHLFD 65
           +P ++L G GA  ++   +      K L+VTD  L K GL D + S + E   +   +FD
Sbjct: 12  IPTVTLMGIGAHKEVGRQIKVLGGKKPLLVTDKGLTKAGLTDQIRSLIKEDTGIDVVVFD 71

Query: 66  EVFPNPTEELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAYSGVGKV 125
           E  PNPT++ V  G   ++   CD II+ GGGS  D AK + IL  N G    Y G+ K 
Sbjct: 72  ETVPNPTDKNVHDGLKVFKDNGCDMIISLGGGSSHDCAKGIGILATNGGNIRNYEGIDKA 131

Query: 126 KNAGVPLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLEIPAS 185
                P +AINTTAGTA+EMT   +I ++  KVK  I+D  + P++A++D  +M+ +P +
Sbjct: 132 TKPMPPFIAINTTAGTASEMTRFCIITNTDTKVKMAIVDWRVTPNVAINDPLLMMGMPPA 191

Query: 186 VTAATGMDALTHAVEAYVSVGAHPLTDANALEAIRLINLWLPKAVDDGHNLEAREQMAFG 245
           +TAATGMDALTHAVEAYVS  A P+TDA AL+AIRLI+ +L  AV +G ++EAR++MA+ 
Sbjct: 192 LTAATGMDALTHAVEAYVSTLATPVTDACALQAIRLISKYLRSAVANGSDIEARDKMAYA 251

Query: 246 QYLAGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFARIAQA 305
           +YLAGMAFN+A LG VHA+AHQ G  ++LPHGVCNAILLP VE FN    + RFA IA A
Sbjct: 252 EYLAGMAFNNASLGYVHAMAHQLGGFYDLPHGVCNAILLPHVERFNLIAKLDRFADIAVA 311

Query: 306 MGVETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKALADPCAPCN 365
           MG    G+S   A+++A+ AI  LS+ VGIP G  +LGV KEDI      A+ D C   N
Sbjct: 312 MGENVEGLSPRDAAEKALQAIEKLSRDVGIPGGLKELGVKKEDIPTMAQNAMKDACGLTN 371

Query: 366 PRTASRDEVRGLYLEAL 382
           PR A+ +++  +Y  AL
Sbjct: 372 PRRATLEDIIMIYENAL 388


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: 367
Number of extensions: 13
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: 382
Length of database: 388
Length adjustment: 30
Effective length of query: 352
Effective length of database: 358
Effective search space:   126016
Effective search space used:   126016
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 24 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