GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Laceyella sediminis RHA1

Align Aconitate hydratase A; ACN; Aconitase; (2R,3S)-2-methylisocitrate dehydratase; (2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate dehydratase; Iron-responsive protein-like; IRP-like; Probable 2-methyl-cis-aconitate hydratase; RNA-binding protein; EC 4.2.1.3; EC 4.2.1.99 (characterized)
to candidate WP_022736982.1 CLV36_RS07505 aconitate hydratase AcnA

Query= SwissProt::Q5SMF6
         (902 letters)



>NCBI__GCF_003003125.1:WP_022736982.1
          Length = 907

 Score = 1109 bits (2869), Expect = 0.0
 Identities = 558/902 (61%), Positives = 683/902 (75%), Gaps = 5/902 (0%)

Query: 5   FQTLKTLTTKSGTYGYYDLQELERKGVAEVSRLPFSIRVMLESLLRNEDGYQVTREDIEA 64
           F     L      Y YY L  LE +G+  VSRLPFSI+V+LE+ +R  DG  VT+E IE 
Sbjct: 6   FHVRSKLKVGEQEYVYYRLNGLEEQGIGPVSRLPFSIKVLLEAAVRQYDGKAVTKEHIEQ 65

Query: 65  LARWRPDPGEINVPLKLARVILQDFTGVPAVVDLAAMRDAIKAKGGDPKRINPVVPADLV 124
           LA W     +  +  K AR++LQDFTGVPAVVDLAA+R A+   GGDP+RINP++P DLV
Sbjct: 66  LATWADKRSDKEIAFKPARIVLQDFTGVPAVVDLAALRSAMARVGGDPERINPLIPVDLV 125

Query: 125 IDHSVQVDAFGTAYAFFYNVEKEYERNRERYLLLKWAQNALENFRVVPPGTGIVHQVNIE 184
           IDHSV VD  GT  A  YN+  E+ERN ERY LL+WA  +L+NFR VPP TGIVHQVN+E
Sbjct: 126 IDHSVMVDKAGTQDALEYNMNLEFERNEERYRLLRWAAESLDNFRAVPPATGIVHQVNLE 185

Query: 185 YLTKVVMTGKRDGLTLAFPDSLVGTDSHTTMVNGLGVLGWGVGGIEAEAVMLGQPYYMLA 244
           YL  V  T + DG T+ FPDSLVGTDSHTTM+NGLGV+GWGVGGIEAEA MLGQP Y + 
Sbjct: 186 YLANVAATREVDGETVVFPDSLVGTDSHTTMINGLGVVGWGVGGIEAEACMLGQPLYFIT 245

Query: 245 PRVVGFKLYGELPEGATATDLVLTVTEMLRKHGVVGKFVEFYGPGVAKLSTPDRATIANM 304
           P V+GFKL G+LP+GATATDL LTVTEMLRK GVVGKFVEFYGPG++ LS  DRAT+ANM
Sbjct: 246 PEVIGFKLTGQLPDGATATDLALTVTEMLRKKGVVGKFVEFYGPGLSNLSLADRATVANM 305

Query: 305 APEYGATMGFFPVDEETLNYLRQTGRPEELVELVEAYTKAVGLFRTPEAEEKVQYSEYLE 364
           APEYGAT+GFFPVD+E LNYLR TGR EELV LV+ Y +A GLFRT +  + V +++ +E
Sbjct: 306 APEYGATIGFFPVDDEALNYLRNTGRDEELVTLVKEYYQAQGLFRTDDTPDPV-FTDTVE 364

Query: 365 LDLSAVEPSLAGPKRPQDRVPLKEVKKSFLAHLTKPVKERGFGLSEDQLQRKVLVKRRD- 423
           LDLS V PSL+GPKRPQDR+ L  +K+++   L KP+ +RGFGLSE++  +   V   D 
Sbjct: 365 LDLSTVVPSLSGPKRPQDRIELTAMKEAWNETLRKPIDQRGFGLSEEECAKSAQVSLPDG 424

Query: 424 EEFELTHGSVVIAAITSCTNTSNPSVMLGAGLLAKKAVEAGLDRKPWVKTSLAPGSKVVT 483
             ++L  G+VVIAAITSCTNTSNPSVM+GAGL+AKKAVE GL  KP+VK+SL PGSKVVT
Sbjct: 425 STYQLDQGAVVIAAITSCTNTSNPSVMVGAGLVAKKAVEKGLTVKPFVKSSLTPGSKVVT 484

Query: 484 DYLEMSGLMPFLEALGFHLVGYGCTTCIGNSGPLPEDIAKAVEEGNLVVAAVLSGNRNFE 543
           DYL+ +GL+  L  LGF + GYGC TCIGNSGPL ++++KA+EE +L VA+VLSGNRNFE
Sbjct: 485 DYLDKAGLIEPLAKLGFTVAGYGCATCIGNSGPLSDEVSKAIEENDLTVASVLSGNRNFE 544

Query: 544 GRINPHVKANYLASPMLVVAYALAGRMDIDFTTEPLGFDPNGKPIYLKDIWPSMEEIREA 603
           GRI+P VKANYLASP LVVAYALAG ++IDF TEP+G +  G+ IYLKDIWPS  EI + 
Sbjct: 545 GRIHPLVKANYLASPPLVVAYALAGTVNIDFATEPIGHNDAGEAIYLKDIWPSSHEISQV 604

Query: 604 IRKTLDPELFKKEYSKVFEGDERWQALPAPTGELYQWDPESTYIQNPPFFEDLGE--RKV 661
           +   +  E F+K+Y++VF+ +ERW  LP P G LY+WD +STYIQ PPFF D+     ++
Sbjct: 605 MNSAISAEQFRKQYAQVFDANERWNQLPTPKGVLYEWDQDSTYIQEPPFFVDMSADVEEI 664

Query: 662 EDIRGARVLLVLGDSVTTDHISPAGAIPVKSPAGQYLISKGVKPEDFNSYGSRRGNHEVM 721
           + I GA +L +L DSVTTDHISPAG+I   SPAG+YL  KGV  +DFNSYGSRRGN  VM
Sbjct: 665 KPITGAHILALLNDSVTTDHISPAGSIAPTSPAGRYLQDKGVAIKDFNSYGSRRGNDRVM 724

Query: 722 MRGTFANIRIKNLMLDGIEGGYAKKLPEGDVDFVYNVAMRYKAEGTPLLVIAGKEYGTGS 781
            RGTFANIRI+N M+ G EGG  K +P   V  +Y+ AM YK  GTPL+VIAGKEYGTGS
Sbjct: 725 TRGTFANIRIRNQMVPGSEGGVTKHVPSQQVMSIYDAAMEYKKSGTPLVVIAGKEYGTGS 784

Query: 782 SRDWAAKGTYLLGIRAVLAESFERIHRSNLVGMGVLPLEFLPGENRETLGLTGYEVYDIL 841
           SRDWAAKGT LLG++AV+AESFERIHRSNLVGMGVLPL+F  G N ++LGL G E  DI 
Sbjct: 785 SRDWAAKGTNLLGVKAVIAESFERIHRSNLVGMGVLPLQFANGANWQSLGLDGTEKIDIA 844

Query: 842 GLED-LKPRKLVDIVARREDGSEVRFQAIARLDTPVEVDYYKNGGILQTVLLNMLKEAKA 900
           GL D + P + + + A + DGS V+F    RLD+ V+++YY+NGGILQTVL  +L   + 
Sbjct: 845 GLNDEVTPGQTLTVTATKPDGSSVQFDVTVRLDSVVDIEYYRNGGILQTVLRQILANQEG 904

Query: 901 TE 902
           ++
Sbjct: 905 SK 906


Lambda     K      H
   0.317    0.137    0.399 

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: 2153
Number of extensions: 84
Number of successful extensions: 5
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: 902
Length of database: 907
Length adjustment: 43
Effective length of query: 859
Effective length of database: 864
Effective search space:   742176
Effective search space used:   742176
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.

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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