GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Geobacter metallireducens GS-15

Align L-lactaldehyde reductase (EC 1.1.1.77) (characterized)
to candidate WP_004513219.1 GMET_RS05235 alcohol dehydrogenase

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



>NCBI__GCF_000012925.1:WP_004513219.1
          Length = 387

 Score =  310 bits (795), Expect = 3e-89
 Identities = 174/381 (45%), Positives = 237/381 (62%)

Query: 2   SFMLALPKISLHGAGAIADMVNLVANKQWGKALIVTDGQLVKLGLLDSLFSALDEHQMSY 61
           +F   +P ++L G G+  +    V      KAL+VTD  +  +G+ D +   ++   ++ 
Sbjct: 7   TFGFFIPTVTLMGVGSSKETGAQVKALGARKALLVTDKGISAMGMADQIKQQVEAAGVAV 66

Query: 62  HLFDEVFPNPTEELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAYSG 121
            +FD   PNPT+  V  G   YQ   CD II+ GGGS  D AK V ++  N G    + G
Sbjct: 67  VIFDGAEPNPTDTNVHDGVKVYQENGCDSIISLGGGSSHDCAKGVGLVIGNGGHIRDFEG 126

Query: 122 VGKVKNAGVPLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLE 181
           V K      P VAINTTAGTA+EMT   +I ++   VK  I+D    P+IA++D  +ML 
Sbjct: 127 VNKSTKPMPPFVAINTTAGTASEMTRFCIITNTDTHVKMAIVDWRCTPNIAINDPVLMLG 186

Query: 182 IPASVTAATGMDALTHAVEAYVSVGAHPLTDANALEAIRLINLWLPKAVDDGHNLEAREQ 241
            PA +TAATGMDALTHAVEAYVS  A P+TDA AL+AI+LI  +L  AV +G NLEAR++
Sbjct: 187 KPAPLTAATGMDALTHAVEAYVSTIATPITDACALQAIKLIAEYLSPAVANGDNLEARDR 246

Query: 242 MAFGQYLAGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFAR 301
           MA+ +YLAGMAFN+A LG VH++AHQ G  +NLPHGVCNAILLP V  FN      R+A 
Sbjct: 247 MAYAEYLAGMAFNNASLGYVHSMAHQLGGFYNLPHGVCNAILLPAVSEFNAIACPKRYAD 306

Query: 302 IAQAMGVETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKALADPC 361
           IA A+G +  G++   A+ +AI AIR LS  +GIP G  +L V +ED++   + A  D C
Sbjct: 307 IAVALGEDITGLAPLDAAAKAIAAIRKLSAAIGIPAGLKELNVKEEDLKVMAENAKKDAC 366

Query: 362 APCNPRTASRDEVRGLYLEAL 382
              NPR A+ ++V G++  A+
Sbjct: 367 QLTNPRKATLEQVIGIFKAAM 387


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: 381
Number of extensions: 10
Number of successful extensions: 1
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: 387
Length adjustment: 30
Effective length of query: 352
Effective length of database: 357
Effective search space:   125664
Effective search space used:   125664
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