GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Paraburkholderia bryophila 376MFSha3.1

Align isobutyryl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate H281DRAFT_01204 H281DRAFT_01204 hypothetical protein

Query= reanno::pseudo3_N2E3:AO353_25670
         (383 letters)



>FitnessBrowser__Burk376:H281DRAFT_01204
          Length = 377

 Score =  550 bits (1418), Expect = e-161
 Identities = 267/372 (71%), Positives = 323/372 (86%)

Query: 7   TEEQVMIRDMARDFARGEIAPHAQAWEKAGWIDDALVAKMGELGLLGMVVPEEWGGTYVD 66
           TEEQ MIRD ARDFA   +AP+A  W++   +   +V +MG+LG LGM+VP +WGG+Y D
Sbjct: 6   TEEQRMIRDAARDFATERLAPNAAQWDRDAQLPADVVRQMGDLGFLGMIVPSQWGGSYTD 65

Query: 67  YVAYALAVEEISAGDGATGALMSIHNSVGCGPVLNYGTEEQKQTWLADLASGQAIGCFCL 126
           YVAYALA+EEI+AG  A   LMS+HNSVGCGP+LN+G++ QK  +L DLA+G+ IG FCL
Sbjct: 66  YVAYALALEEIAAGCAACATLMSVHNSVGCGPILNFGSDAQKDRYLHDLATGRRIGAFCL 125

Query: 127 TEPQAGSEAHNLRTRAELRDGQWVINGAKQFVSNGRRAKLAIVFAVTDPDLGKKGLSAFL 186
           TEPQAGSEA+NLRTRA L DG+W++NG+KQFV+NG RA +AIVFAVTDPD GK+GLSAF+
Sbjct: 126 TEPQAGSEANNLRTRAVLCDGKWILNGSKQFVTNGARADIAIVFAVTDPDRGKRGLSAFI 185

Query: 187 VPTDTPGFIVDRSEHKMGIRASDTCAVTLNNCTIPEANLLGERGKGLAIALSNLEGGRIG 246
           VPTDTPGF V + EHK+GIRASDTC ++L++C +P+ANLLGE G+GL IALSNLEGGRIG
Sbjct: 186 VPTDTPGFNVGKPEHKLGIRASDTCPISLDDCAVPDANLLGEPGEGLRIALSNLEGGRIG 245

Query: 247 IAAQALGIARAAFEAALAYARDRVQFDKPIIEHQSVANMLADMHTRLNAARLLILHAARL 306
           IAAQA+GIARAAF+AA AYA +R+QF K + +HQ++ANMLADM TRLNAARLL+ HAARL
Sbjct: 246 IAAQAVGIARAAFDAARAYASERMQFGKALKDHQTIANMLADMATRLNAARLLVHHAARL 305

Query: 307 RSAGKPCLSEASQAKLFASEMAEKVCSSAIQIHGGYGYLEDYPVERYYRDARITQIYEGS 366
           RSAG+PCLSEASQAKLFASE+AE+VCS+AIQIHGGYGYLEDY VER+YRDARITQIYEG+
Sbjct: 306 RSAGEPCLSEASQAKLFASEVAEEVCSNAIQIHGGYGYLEDYAVERHYRDARITQIYEGT 365

Query: 367 SEIQRMVIAREL 378
           SE+QRMVIAR +
Sbjct: 366 SEVQRMVIARHV 377


Lambda     K      H
   0.319    0.134    0.394 

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: 451
Number of extensions: 12
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: 383
Length of database: 377
Length adjustment: 30
Effective length of query: 353
Effective length of database: 347
Effective search space:   122491
Effective search space used:   122491
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: 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