GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Desulfitobacterium hafniense DCB-2

Align Respiratory FAD-dependent D-lactate dehydrogenase Dld; EC 1.1.2.4 (characterized, see rationale)
to candidate WP_015944483.1 DHAF_RS16125 FAD-binding oxidoreductase

Query= uniprot:Q8EGS3
         (934 letters)



>NCBI__GCF_000021925.1:WP_015944483.1
          Length = 978

 Score =  766 bits (1978), Expect = 0.0
 Identities = 393/920 (42%), Positives = 567/920 (61%), Gaps = 11/920 (1%)

Query: 24  DPVRRFAWSTDASYFRIVPEVVVHAETLEQVKLTLTVARKHNAPVTFRAAGTSLSGQAIG 83
           DP+    +  DAS++R++P++V+      ++   L ++++   PVTFR AGTSLSGQA+ 
Sbjct: 56  DPLYTLGYGIDASFYRLIPKIVIRVLNDAEMGEILRLSQRTKIPVTFRTAGTSLSGQALT 115

Query: 84  EGILLILGHDGFRKIEVSSDAKQITLGAAVIGSDANAVLAPLNRKIGPDPATIASAKIGG 143
           + +LL+L    +R  ++    K+I+L   ++G +AN  L    RKIGPDPA+I    IGG
Sbjct: 116 DSVLLVL-QGSWRHYKIHDHGKKISLEPGILGVEANRYLRSYKRKIGPDPASIDHCMIGG 174

Query: 144 IVANNASGMCCGTAQNSYQTIASAKLLFADGTELDTGCEKSKAEFAKTHGKLLQDLSELS 203
           I ANNASGMCCGT+ NSY+T+   +++F DGT LDTG   S+  F +  G+L++ + E+ 
Sbjct: 175 IAANNASGMCCGTSDNSYKTVDEMRIIFDDGTVLDTGDSSSRQYFRERKGELIRQIEEIR 234

Query: 204 HLTRHNSALAERIRKKYSIKNTTGYGINSLIDFTDPFDIINHLMVGMEGTLAFINEVTYH 263
                +  L   I+KKY IKNTTGY IN+ +DF DP +II H+++G EGTL FI+E+TY 
Sbjct: 235 DELNADPDLVAMIKKKYKIKNTTGYSINAFVDFQDPIEIIKHILIGSEGTLGFISEITYK 294

Query: 264 TVNEAKFKASAMAVFHNMEDAARAIPLINGESVSAAELLDWPSIKAVTGKPGMPDWLSEL 323
           TV +   KASA+ ++ +M+ A RA+  ++ + V+AAE++D PS+++V   PGMPD+L  L
Sbjct: 295 TVVDYDHKASALIMYPDMDHACRAVMKLDRDLVAAAEMMDRPSLRSVEDAPGMPDYLKSL 354

Query: 324 PALSAILLIESRADDAQTLEHYTQDVTAKLAGFDFIRPMEFSTNPAVYDKYWAMRKGLFP 383
              +  LL+E R  + + LE   ++ TA L     I P+ F++  + Y+ YW +RK +FP
Sbjct: 355 SDTATALLVEVRGANPEELEQRIKNATAVLEDIPTIFPISFTSVKSEYETYWKIRKDIFP 414

Query: 384 IVGGERPKGTSVIIEDVAFELEHLAAAAHDITELFHKHGYPEGCIYGHALAGNFHFIITP 443
            VGG R +GT+V+IEDVAF LE LA A  D+ +  +K GY +  IYGHAL GN+HFI TP
Sbjct: 415 AVGGVRAQGTAVLIEDVAFPLERLAEATADLRDSLNKFGYTDAIIYGHALDGNWHFIFTP 474

Query: 444 AFTTQADIDRFHAFMDDIADMVINKYNGSMKAEHGTGRAVAPFVEKEWGQDAYTLMKNIK 503
            F +  +I R+   M+++ + V+ KYNGS+KAEHGTGR +APFVE EWG   Y LMK IK
Sbjct: 475 KFDSDEEIARYEGLMNEVNEFVVKKYNGSLKAEHGTGRNMAPFVELEWGSKTYELMKRIK 534

Query: 504 QVFDPQGILNPGVILNDDSNIHVKNIKPCPVVDDFVDKCIECGFCEKTCPTSALNFSPRQ 563
             FDP  +LNPGVI+ND+ N++++N+K  P   D +D+C  CGFC+  CP+  L  +PR 
Sbjct: 535 SAFDPHNLLNPGVIINDNKNVYLENLKAMPASHDTIDRCTNCGFCQDICPSKHLTTTPRM 594

Query: 564 RIATLREIERLEQSG-DKAAAAKMRADAKYDVIDTCAACQLCTIACPVDNSMGQLVRKLR 622
           RI   REI  L+++G D     ++  D  Y    TCA   LC  +CP++ + G   + LR
Sbjct: 595 RIILQREISDLKRTGRDPKRLMRLLRDYDYAGNATCATDGLCATSCPLNINTGDNTKYLR 654

Query: 623 TPYISTTEQKVLDFQAKHFGAVNQVISTGFDVLGVIHKITGDGITNALMKTGRLISK-EV 681
           +  I+   +KV    AK+   V  ++  G   +  +H   G  I   + +T R +S+ ++
Sbjct: 655 SRAITPATRKVARALAKNMNGVTGIMRFGLGAVDGVHGFLGTRILGGMARTARDVSQSKI 714

Query: 682 PYWNPDFPKGGK---LPKPSPAKA-GQET--VVYFPACGGRTFGPTPKDPDNRTLPEVVV 735
           P WN   P  GK    P+P  A A G E   VVYFP+C  R+ GP  KD D R L EV+ 
Sbjct: 715 PLWNEWMPSKGKGKVRPRPPFASAQGGEVLKVVYFPSCISRSMGPARKDKDQRPLNEVMC 774

Query: 736 TLLERAGYNVITPEKTRDLCCGQMWESKGDFKNADAKRQELIDVLSKMSNGGKIPVLVDA 795
           +LL +AGY VI P     LCCG  WESKG F  AD K  EL  VL + S  GK P++ D 
Sbjct: 775 SLLAKAGYEVIIPPGLDKLCCGMPWESKGFFDIADEKSAELEKVLLQASENGKYPIVCDT 834

Query: 796 LSCTYRTLTG-NPQVQITDLVEFMHDKLLDKLSINK-KVNVALHLGCSARKMKLEPKMQA 853
             C YR        +++ + VEF HD LL +L I K +  +A+H+ CS+ KM+L  K +A
Sbjct: 835 SPCLYRMKRAFTSGIELHESVEFTHDFLLHRLKIKKARETIAVHVTCSSVKMRLSEKFKA 894

Query: 854 IANACSAQVLKPAGIECCGYAGEKGLYKPEINASALRNIKKLIPVEVKEGYYANRMCEVG 913
           +A AC+ +V+ P  + CCG+AG+KG   PE+N +AL  +   +P     GY  +R CE+G
Sbjct: 895 LAEACAEKVIIPDDVHCCGFAGDKGFTYPELNDAALAGLNGALPDNCAGGYSNSRTCEIG 954

Query: 914 LTQHSGISYRHLAYLLEECS 933
           L+ HSGISY+ L YL++ CS
Sbjct: 955 LSAHSGISYQSLIYLVDRCS 974


Lambda     K      H
   0.319    0.135    0.402 

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: 2025
Number of extensions: 74
Number of successful extensions: 7
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: 934
Length of database: 978
Length adjustment: 44
Effective length of query: 890
Effective length of database: 934
Effective search space:   831260
Effective search space used:   831260
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 (21.7 bits)
S2: 57 (26.6 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