Alignments for a candidate for drdehyd-beta in Acidovorax sp. GW101-3H11

GapMind for catabolism of small carbon sources

Alignments for a candidate for drdehyd-beta in Acidovorax sp. GW101-3H11

Align 2-deoxy-D-ribose dehydrogenase β subunit (characterized)
to candidate Ac3H11_2239 Isoquinoline 1-oxidoreductase beta subunit (EC 1.3.99.16)

Query= metacyc::MONOMER-20833
         (739 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2239
          Length = 759

 Score =  361 bits (926), Expect = e-104
 Identities = 268/747 (35%), Positives = 388/747 (51%), Gaps = 50/747 (6%)

Query: 9   DAPVNLSRRRFLASTAVGALVIGFGLPLGAGRVQAATSAERGT----QVPAFLEIRPDGT 64
           DA   ++RR FL  TA     +G   PL A    A  +A  G     Q  AF+ I  DGT
Sbjct: 36  DAADGMARRTFLKVTAASGFALG-AFPLAATAQGAGAAAPAGLKPHEQPSAFVRIDADGT 94

Query: 65  VRLLSPFMEGGQGTHTAMAQIVGEELDADPATFIVEAAPPGEAYVVMENGLRITGGSMSV 124
           V +    ++ GQG  T +  I+ EELDAD +           AY     G+ +TGGS S+
Sbjct: 95  VTVTINRLDFGQGVQTGLPMILAEELDADWSKVRSVHGDANPAYADPAFGMHLTGGSNSI 154

Query: 125 RMSYPTMRRLGALARAMLLQAGAKQWGVPVGELTTQPGRVVHAASGRSLGYGELASSALD 184
           + SY   R LGA  RAML+ A A QWGV    L T  G VV    G+ LGYG LA +A+ 
Sbjct: 155 KNSYTQYRELGARTRAMLVGAAAAQWGVDASALRTSNGFVV-GPGGKKLGYGALAEAAMK 213

Query: 185 MPVPDPASITLRDPSQFRWIGKPVKRLDAYDKSTGKALYSIDLKVDNMLHAAVQHAPRLG 244
            PVP+   +TL+DP QFR IGKP  RLDA  KS+G+  Y ID+++  ML A V   P  G
Sbjct: 214 QPVPE--KVTLKDPKQFRIIGKPTGRLDAKAKSSGQQDYGIDVRLPGMLTAVVARPPVFG 271

Query: 245 MTVGSLRNQSQVEGMKGVHSVHVLP-----GAVAVVAERWWHAKRAVEAIQVDWQEAAAD 299
               SL + S  + +KGV +V  +P       VA++A+ +W AK+  +A++V+W  +A  
Sbjct: 272 AKPKSL-DDSAAKAIKGVKAVLRVPTDRGGEGVAIIADGYWPAKQGRDALKVEWDTSA-- 328

Query: 300 SALRVMPADFSS--DKHREFLAAQQGPTRDDENEGDVAGALKGAKTQVEATYHNQYLNHA 357
               V   D ++   ++RE LAA+ G   +   + D+A  L GA  ++ A +   YL HA
Sbjct: 329 ----VAKPDTTALLAQYRE-LAAKPG---NVAMQADMA-PLAGAAHKISAEFVFPYLAHA 379

Query: 358 QLEPPSALARFNPDGTLEIWLPNQAPDMFRADIAKRTGLDPAQITLHSPLLGGFFGRHFL 417
            +EP +   + + D   E+W+  Q P +     AK  GL P  + +++ + GG FGR  +
Sbjct: 380 PMEPLNCTVKLDAD-KAELWMGTQMPGLDAMAAAKTLGLQPQNVKVNTQMAGGGFGRRAI 438

Query: 418 YDSANPYPQAIALAKA-----VSRPIKLIWSREEEFLRDVLRPLAVVKFRAALDDKGLPV 472
             +++   +A  +AKA     ++ P++ +WSRE++      RP+ V +     D +G  +
Sbjct: 439 -PTSDYVVEACGVAKAARTVGITAPVRTLWSREDDIKGGYYRPMHVHRAEIGFDAQGKVL 497

Query: 473 A----IEAVSATEG-PTEALAGKQGDKIDPTAVEGLSGKSYAIPNKRIAQIYVKGAPMLG 527
           A    I   S T+G P EA   K G  ID TA+EG+  + Y +P K          P+L 
Sbjct: 498 AWDHSIVGQSITKGSPFEAFMVKNG--IDATAIEGMK-EPYDLPMKLTVHHPDVNVPVL- 553

Query: 528 YWRSVGNSLNDFFYESFLDELADKGGHDPYELRLHLLRD-NPRLTTLLQAAGELSGGWKR 586
           +WRSVG++   +  E+ +DE+A     DP   R+ L+ D +PR    LQ A   SG  K+
Sbjct: 554 WWRSVGSTHTAYVMETLIDEVARATKQDPVAYRMALMGDKHPRHKAALQLAVAQSGYGKK 613

Query: 587 GPFTAEDGTRRARGVAMASPFGSHTAAIAEVSIENGKVKVHDIWQAIDPGSIVNPAIVEA 646
                +    RA GVA+   F S  A + E S+++G  K+H I   +    +VNP  VEA
Sbjct: 614 -----KLAAGRAWGVAVHESFQSVVAYVVEASVKDGTPKLHSITAGVHCNLVVNPKSVEA 668

Query: 647 QVNGAVALGLSQTLLEEAVYV-DGKPRARNYDLYPILAPAQMARVHVRVVESGEKMGGIG 705
           QV G   +GLS  L   A+ + DG     N+  + +     M +V V +V S E   G+G
Sbjct: 669 QVQGGALMGLSMCLPGAAITLKDGVVEQSNFGDFAVPRITDMPQVAVHIVPSAEPPTGMG 728

Query: 706 EPPLPAVAPAVANAVAQLTGQRVRSLP 732
           EP LP +APA ANAVA+LTG+  R LP
Sbjct: 729 EPGLPPLAPAFANAVARLTGKTPRELP 755


Lambda     K      H
   0.317    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: 1425
Number of extensions: 83
Number of successful extensions: 12
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: 739
Length of database: 759
Length adjustment: 40
Effective length of query: 699
Effective length of database: 719
Effective search space:   502581
Effective search space used:   502581
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: 55 (25.8 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources