GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Lacinutrix algicola AKS293

Align Aconitate hydratase B; ACN; Aconitase; EC 4.2.1.3; (2R,3S)-2-methylisocitrate dehydratase; (2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate dehydratase; 2-methyl-cis-aconitate hydratase; EC 4.2.1.99; Iron-responsive protein-like; IRP-like; RNA-binding protein (uncharacterized)
to candidate WP_055435324.1 ASC41_RS03870 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= curated2:Q9ZL64
         (852 letters)



>NCBI__GCF_001418085.1:WP_055435324.1
          Length = 924

 Score =  299 bits (766), Expect = 4e-85
 Identities = 275/917 (29%), Positives = 433/917 (47%), Gaps = 119/917 (12%)

Query: 7   DYKKSVLERKSEGIPPLPLNAKQVEAVVEILMKDPTNAAFAKEL--LIHRVSPGVDEGAK 64
           DY K +  RK +G+ P P++  ++ + +   +KD  N    + L   I+ V PG    A 
Sbjct: 6   DYLKQIENRKEQGLHPQPIDGAELLSQIIEQIKDLDNEHREESLNFFIYNVLPGTTSAAT 65

Query: 65  VKAEFLAQLSQKKLECPHISALEATTLLGTMLGGYNVEPLIVGLESQDKNIAKESAKALK 124
           VKA+FL ++   +     I+   A   L  M GG +V+ L+      D ++AK+SA+ LK
Sbjct: 66  VKAKFLKEIILGESIVKEITPTFALEQLSHMKGGPSVKVLLDIALGNDADLAKQSAEILK 125

Query: 125 TTLLVY-GSFDKIAAMSKTNA-LAKEVLESWANAEWFLNKEPLNECIEACVFKID-GETN 181
           T + +Y    D++    K+ + +AK+++ES+A AE+F     ++E IE   +    G+ +
Sbjct: 126 TQVFLYEADTDRLEEAFKSGSEIAKDIIESYAKAEFFTKLPEIDEKIEVVTYIAGVGDIS 185

Query: 182 TDDLSPASDAFTRSDIPLHAKAMLKNRIENYEQRIEAIKT----KGVPVAYVGDVVGTGS 237
           TD LSP  DA +RSD  LH + M ++  ++ +  + A+K     K V +      +G GS
Sbjct: 186 TDLLSPGGDAHSRSDRELHGQCMFEHN-KDMQNELLALKEQHPDKRVMLIAEKGTMGVGS 244

Query: 238 SRKSATNSI-MWH---FGKDIPFVPNKRSGGIVIGGV--IAPIFFATCEDSGAL------ 285
           SR S  N++ +W    F K +PF+    +   VI G   IAPIF  T   +G +      
Sbjct: 245 SRMSGVNNVALWTGVPFSKYVPFI----NFAPVIAGTNGIAPIFLTTVGVTGGIGLDLKN 300

Query: 286 ------------------PIVADVKDLKEGDIIKIYPYKGEITLNDKVVSTFK--LEPET 325
                             PI+ +   +  G I+ I   + ++   DK +        P+ 
Sbjct: 301 WVQQKDAEGNTVRDEDGEPILKETYSVATGTILTINTKEKKLYNGDKELKDISAAFTPQK 360

Query: 326 LLDEVRASGRIPLIIGRGLTNKARKFLGLGESEAFKKPSAPKSDAKGYTLAQKIVG-HAC 384
           + + ++A G   ++ G+ L   A K LG+   + +        + +G T  +KI   +A 
Sbjct: 361 M-EFMKAGGSYAVVFGKKLQTFAAKALGIEAPQVYATAKEVSIEGQGLTAVEKIFNKNAV 419

Query: 385 GVKG--ILPGAYCEPKVTTVGSQDTTGAMTRDEVKELASLKFDAPFV---LQSFCHTAAY 439
           G  G  +  G+Y   +V  VGSQDTTG MT  E++ +A+    +P V    QS CHTA+ 
Sbjct: 420 GTSGATLHAGSYVRAEVNIVGSQDTTGLMTSQELEMMAATVI-SPIVDGAYQSGCHTASV 478

Query: 440 PKPSDVSLHATLP---------GFITQRGGVALH-PGDGVIHTWLNRMGLPD-TLGTGGD 488
               D    A +P         G IT R     + P   VIH  LN + + D  +  GGD
Sbjct: 479 ---WDDKSKANIPRLMSFMNDFGLITGRDPKGKYFPMTDVIHKVLNDITVGDWDIIIGGD 535

Query: 489 SHTRFPLGISFPAGSGLVAFAAVTGTMPLNMPESVLVRFKGEMNPGITLRDLVNAIPYYA 548
           SHTR   G++F A SG VA A  TG   + +PESV V FKG+M   +  RD+V+A     
Sbjct: 536 SHTRMSKGVAFGADSGTVALALATGEASMPIPESVKVTFKGQMKSYMDFRDVVHATQQQM 595

Query: 549 IKKGLLTVEKKGKINVFNGRILEIEGLPDIKMEQAFELSDASAERSAAACVVRLNKEPMI 608
           +K       + G  NVF GR++E+  +  +  ++AF  +D +AE  A A +     + +I
Sbjct: 596 LK-------QFGGENVFQGRVIEVH-IGTLTADEAFTFTDWTAEMKAKASICISEDDTLI 647

Query: 609 EYLKSNIKLIDEMIASGYED-KETLKKRRDAMQAWV------DKPVLLEPDSNAQYAAVI 661
           E L+     I  MI  G ++ K+ LK   D  +  +       KP  L PD+NA+Y A +
Sbjct: 648 ESLEIAKGRIQIMIEKGMDNAKQVLKGLVDKAETRIIELKTGMKP-SLRPDANAKYHAEV 706

Query: 662 EIDVAEITEPILACPN-DPDDVA---TLSEVLADTTGKRPHAIDEVFIGSCMTNIGHFRA 717
            ID+ +I EP++A P+ + +DV+   T   +   +       +D  F+GSCM + G  + 
Sbjct: 707 IIDLDQIVEPMIADPDVNNEDVSKRYTHDNIRPLSYYGGTKKVDLGFVGSCMVHKGDMKI 766

Query: 718 FGEIVKNAPPS------QARLWVVPPSKMDEQELINEGYYAIF------------GAAGA 759
             +++KN          +A L V PP+     EL  EG + +                 A
Sbjct: 767 LAQMLKNVEAQYGKVEFKAPLIVAPPTYNIVDELKAEGDWEVLVRYSGFEFDDNAPKGEA 826

Query: 760 RT--------EVPGCSLCMGNQARVRDNAVVFSTSTRNFDNRMGRGA-----KVYLGSAE 806
           RT        E PGC+LCMGNQ +      V +TSTR F  R+ + +     +  L S  
Sbjct: 827 RTGYENMLYLERPGCNLCMGNQEKAAPGDTVMATSTRLFQGRVVKDSGEKKGESLLSSTP 886

Query: 807 LGAACALLGRIPTKEEY 823
           +     +LGR PT EEY
Sbjct: 887 VVVLSTILGRTPTMEEY 903


Lambda     K      H
   0.317    0.135    0.390 

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: 1689
Number of extensions: 85
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: 852
Length of database: 924
Length adjustment: 43
Effective length of query: 809
Effective length of database: 881
Effective search space:   712729
Effective search space used:   712729
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 (21.6 bits)
S2: 56 (26.2 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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