GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Pedobacter sp. GW460-11-11-14-LB5

Align aconitate hydratase (EC 4.2.1.3) (characterized)
to candidate CA265_RS16400 CA265_RS16400 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= BRENDA::P36683
         (865 letters)



>FitnessBrowser__Pedo557:CA265_RS16400
          Length = 921

 Score =  323 bits (829), Expect = 2e-92
 Identities = 288/929 (31%), Positives = 446/929 (48%), Gaps = 118/929 (12%)

Query: 4   EYRKHVAERAAEGIAPKPLD-ANQMAALVELLKNPPAGEEEFLLDLLTNRVPPGVDEAAY 62
           +Y + + +R A+G+ PKP+D A  ++ ++  +KN      E  ++       PG   AA 
Sbjct: 6   DYIQEIEDRKAQGLHPKPIDGAELLSEIITQIKNVNNINREEAVNFFIYNTLPGTTAAAA 65

Query: 63  VKAGFLAAIAKGEAKSPLLTPEKAIELLGTMQGGYNIHPLIDAL--DDAKLAPIAAKALS 120
           VKA FL  I   E     +TP+ A ELL  M+GG +I  L+D    D+   A  AA  L 
Sbjct: 66  VKAQFLKEIILAEVIVAEITPDFAFELLSHMKGGPSIKVLLDIALADNGDKAKKAADVLK 125

Query: 121 HTLLMFDNFYD-VEEKAKAGNEYAKQVMQSWADAEWFLNRPALAEKLTVTVFKV-TGETN 178
             + ++D   D +++    GNE AK++++S+A AE+F   P +AE++ V  F    G+ +
Sbjct: 126 TQVYLYDADTDRLKDAYNNGNEIAKEILESYAKAEFFTKLPEVAEEIKVVTFIAGIGDIS 185

Query: 179 TDDLSPAPDAWSRPDIPLHALAMLK-NAREGIEPDQPGVVGPIKQIEALQQKGFPLAYVG 237
           TD LSP   A SR D  LH   M+   A+E I+  Q     P K +  + +KG       
Sbjct: 186 TDLLSPGNQAHSRSDRELHGKCMITPEAQEEIKALQ--AQHPDKSVMLVAEKG------- 236

Query: 238 DVVGTGSSRKSATNSV-LWFMGDDIPHVPNKRGGGLCLGGK-IAPIFFNTMEDAGALPIE 295
             +G GSSR S  N+V LW      P+VP      +  G   I+PIF  T++  G + I+
Sbjct: 237 -TMGVGSSRMSGVNNVALWTGKRSSPYVPFVNIAPIVGGTNGISPIFLTTVDVTGGIGID 295

Query: 296 VD------------VSN------------LNMGDVIDVYPYKGEVRNHETGELLATFELK 331
           +             + N            +  G V+ +     ++ N E  EL+   +  
Sbjct: 296 LQNWVKKTDENGNVIRNEKDEPILEQRFSVETGTVLTINTKTKKLYNGEQ-ELIDISKAL 354

Query: 332 TDVLIDEVRAGGRIPLIIGRGLTTKAREALGLPHSDVFRQAKDVAESDRGFSLAQKMVGR 391
           T   ++ ++AGG   +I G+ + T A + LG+  S VF  AK+V+   +G +  +K+  R
Sbjct: 355 TPQKMEFMKAGGSYAIIFGKKIQTFAAKTLGIEASSVFAPAKEVSYEGQGLTAVEKIFNR 414

Query: 392 -ACGV---KGIRPGAYCEPKMTSVGSQDTTGPMTRDELKDLACLGFS--ADLVMQSFCHT 445
            A G+   K +  G+    ++  VGSQDTTG MT  EL+ +A    S   D   QS CHT
Sbjct: 415 NAVGLTQGKVLHAGSDVRVEVNIVGSQDTTGLMTAQELEAMAATVISPIVDGAYQSGCHT 474

Query: 446 AA-YPKPVDVNTHHTLPDFIMNRGGVSLRPGDG-------VIHSWLNRMLLPD-TVGTGG 496
           A+ + K    N    L  F+ + G ++ R   G       VIH  LN + + +  +  GG
Sbjct: 475 ASVWDKKAQANIPK-LMKFMNDFGVITARDPKGEYHSMTDVIHKVLNDITIDEWAIIIGG 533

Query: 497 DSHTRFPIGISFPAGSGLVAFAAATGVMPLDMPESVLVRFKGKMQPGITLRDLVHAIPLY 556
           DSHTR   G++F A SG VA A ATG   + +PESV V FKG M+  +  RD+VHA  L 
Sbjct: 534 DSHTRMSKGVAFGADSGTVALALATGEASMPIPESVKVTFKGLMKEHMDFRDVVHATQLQ 593

Query: 557 AIKQGLLTVEKKGKKNIFSGRILEIEGLPDLKVEQAFELTDASAERSAAGCTIKLNKEPI 616
            ++Q          +N+F GRI+E+  +  L  +QAF  TD +AE  A         + +
Sbjct: 594 MLQQ-------FDGENVFQGRIIEVH-IGTLLADQAFTFTDWTAEMKAKASICISQDDTL 645

Query: 617 IEYLNSNIVLLKWMIAEGYGDRRTL--------ERRIQGMEKWLANPELLEADADAEYAA 668
           I+ L      ++ MI +G  +   +         +RI+ ++  +  P L+  D +A+Y A
Sbjct: 646 IQSLEIAKNRIQIMIDKGMDNHNQVLQGLINKANKRIEEIKTGI-KPALM-PDDNAKYYA 703

Query: 669 VIDIDLADIKEPILCAPN----------DPDDARPLSAVQGE-KIDEVFIGSCMTNIGHF 717
            + IDL  I+EP++  P+            D  R L+   G+ K+D  F+GSCM +    
Sbjct: 704 EVVIDLDLIEEPMIADPDVNNADVSKRYTHDTIRDLTFYGGDKKVDLGFVGSCMVHKDDL 763

Query: 718 RAAGKLL-----DAHKGQLPTRLWVAPPTRMDAAQLTEEG------------YYSVFGKS 760
           +   ++L        K +    L VA PT     +L  EG            +     KS
Sbjct: 764 KIVSQMLKNVETQTGKVEFKAPLVVAAPTYNIIDELKAEGDWEYLQKYSGFEFSDALPKS 823

Query: 761 GAR--------IEIPGCSLCMGNQARVADGATVVSTSTRNFPNRL-----GTGANVFLAS 807
            AR        +E PGC+LCMGNQ + A G TV++TSTR F  R+     G      LAS
Sbjct: 824 AARTEYENIMYLERPGCNLCMGNQEKAAKGDTVMATSTRLFQGRVVEDKDGKKGESLLAS 883

Query: 808 AELAAVAALIGKLPTPEEYQTYVAQVDKT 836
             +  ++A++G++P+ EEY+  V  ++ T
Sbjct: 884 TPVVVLSAILGRIPSIEEYKVAVEGINLT 912


Lambda     K      H
   0.317    0.136    0.400 

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: 1666
Number of extensions: 82
Number of successful extensions: 14
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: 865
Length of database: 921
Length adjustment: 43
Effective length of query: 822
Effective length of database: 878
Effective search space:   721716
Effective search space used:   721716
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: 56 (26.2 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