GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Mesorhizobium ciceri WSM1271

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 YP_004140183.1 Mesci_0969 aconitate hydratase 1

Query= SwissProt::P70920
         (906 letters)



>NCBI__GCF_000185905.1:YP_004140183.1
          Length = 896

 Score = 1301 bits (3366), Expect = 0.0
 Identities = 658/905 (72%), Positives = 744/905 (82%), Gaps = 13/905 (1%)

Query: 3   SLDSFKCKKTLKVGAKTYVYYSLPTAEKNGLKGISKLPYSMKVLLENLLRNEDGRSVKKA 62
           SLDSF C++TL  G   Y Y+ L  AEKNGL GIS+LPYSMKVLLENLLRNEDGRSV K 
Sbjct: 4   SLDSFNCRRTLTAGGAEYAYFDLIEAEKNGLTGISQLPYSMKVLLENLLRNEDGRSVTKE 63

Query: 63  DIVAVSKWLRKKSLEH-EIAFRPARVLMQDFTGVPAVVDLAAMRNAMQKLGGDAEKINPL 121
            I AV+ WL  K     EIA+RPARVLMQDFTGVPAVVDLAAMR+AM  LGGD +KINPL
Sbjct: 64  SIQAVAGWLTDKGTAGVEIAYRPARVLMQDFTGVPAVVDLAAMRDAMASLGGDPQKINPL 123

Query: 122 VPVDLVIDHSVIVNFFGDNKAFAKNVTEEYKQNQERYEFLKWGQAAFSNFSVVPPGTGIC 181
           VPVDLVIDHSVIV+ FG   AFA+NV  EY++N+ERY+FLKWGQ AF NF VVPPGTGIC
Sbjct: 124 VPVDLVIDHSVIVDEFGTPMAFARNVELEYERNEERYKFLKWGQQAFRNFRVVPPGTGIC 183

Query: 182 HQVNLEYLSQTVWTKKEKMTVGKKTGTFEVAYPDSLVGTDSHTTMVNGLAVLGWGVGGIE 241
           HQVNLEYL Q VWT  E    G+ T     AYPD+ VGTDSHTTM+NGL VLGWGVGGIE
Sbjct: 184 HQVNLEYLGQVVWTNTED---GETT-----AYPDTCVGTDSHTTMINGLGVLGWGVGGIE 235

Query: 242 AEACMLGQPLSMLLPNVVGFKLKGAMKEGVTATDLVLTVTQMLRKLGVVGKFVEFFGPGL 301
           AEA MLGQP+SMLLP V+GF+L G +KEGVTATDLVLTVTQMLRK GVVGKFVEFFGPGL
Sbjct: 236 AEAAMLGQPVSMLLPEVIGFRLTGKLKEGVTATDLVLTVTQMLRKKGVVGKFVEFFGPGL 295

Query: 302 DHLSVADKATIANMAPEYGATCGFFPVDAAAIDYLKTSGRAAPRVALVQAYAKAQGLFRT 361
            ++++AD+ATI NMAPEYGATCGFFPVD+  I YL  SGR+  R+ALV+AYAKAQGL+R 
Sbjct: 296 SNMTLADRATIGNMAPEYGATCGFFPVDSETIRYLTMSGRSEDRIALVEAYAKAQGLWRE 355

Query: 362 AKSADPVFTETLTLDLADVVPSMAGPKRPEGRIALPSVAEGFSVALANEYKKTEEPAKRF 421
             SADPVFT+ L L+L  VVPSMAGPKRPEGR+AL  + EGF+ A+  EYKK  E +KR+
Sbjct: 356 TGSADPVFTDLLELELGSVVPSMAGPKRPEGRVALEGIPEGFAKAMETEYKKAAEISKRY 415

Query: 422 AVEGKKYEIGHGDVVIAAITSCTNTSNPSVLIGAGLLARNAAAKGLKAKPWVKTSLAPGS 481
           AVEG  +++GHGDVVIAAITSCTNTSNPSVLIGAGLLARNA   GLK KPWVKTSLAPGS
Sbjct: 416 AVEGTDHDLGHGDVVIAAITSCTNTSNPSVLIGAGLLARNANRLGLKQKPWVKTSLAPGS 475

Query: 482 QVVAAYLADSGLQAHLDKVGFNLVGFGCTTCIGNSGPLPEEISKSINDNGIVAAAVLSGN 541
           QVVA YL  SGLQ  LD++GFNLVGFGCTTCIGNSGPLP  ISK+IND G++AAAVLSGN
Sbjct: 476 QVVAEYLEKSGLQKELDQIGFNLVGFGCTTCIGNSGPLPAPISKTINDKGLIAAAVLSGN 535

Query: 542 RNFEGRVSPDVQANYLASPPLVVAHALAGSVTKNLAVEPLGEGKDGKPVYLKDIWPTSKE 601
           RNFEGRVSPDVQANYLASPPLVVAHALAG+VTK+L  EPLGE K+G+PVYLKDIWP+S E
Sbjct: 536 RNFEGRVSPDVQANYLASPPLVVAHALAGTVTKDLTTEPLGEDKNGEPVYLKDIWPSSAE 595

Query: 602 INAFMKKFVTASIFKKKYADVFKGDTNWRKIKTVESETYRWNMSSTYVQNPPYFEGMKKE 661
           I  F++K VT  +F +KYADVFKGD  W+ +K  E +TY W+ +STYVQNPPYF GM   
Sbjct: 596 IQEFIEKNVTRELFARKYADVFKGDEYWQNVKAPEGQTYAWDDNSTYVQNPPYFAGMTSG 655

Query: 662 PEPVTDIVEARILAMFGDKITTDHISPAGSIKLTSPAGKYLSEHQVRPADFNQYGTRRGN 721
              + DI  AR+L +FGDKITTDHISPAGSIK  SPAGKYL++H V  ADFNQYGTRRGN
Sbjct: 656 FGKIGDIKGARVLGLFGDKITTDHISPAGSIKAASPAGKYLTDHGVGVADFNQYGTRRGN 715

Query: 722 HEVMMRGTFANIRIKNFMLKGADGNIPEGGLTKHWPDGEQMSIYDAAMKYQQEQVPLVVF 781
           HEVMMRGTFANIRI+N ML G +G   EGG T H+P  E+ SIYDAAM+Y++E VPLVVF
Sbjct: 716 HEVMMRGTFANIRIRNHML-GENGR--EGGYTIHYPSKEEESIYDAAMEYKREGVPLVVF 772

Query: 782 AGAEYGNGSSRDWAAKGTRLLGVRAVICQSFERIHRSNLVGMGVLPLTFEEGTSWSSLGL 841
           AG EYGNGSSRDWAAKGT LLGVRAVI QSFERIHRSNLVGMGV+P  FEEGTSW+SL L
Sbjct: 773 AGVEYGNGSSRDWAAKGTNLLGVRAVIAQSFERIHRSNLVGMGVIPFVFEEGTSWASLNL 832

Query: 842 KGDEKVTLRGLVGDLKPRQKLTAEIVSGDGSLQRVSLLCRIDTLDELDYYRNGGILHYVL 901
           KGDE V + GL   +KPRQ + A+I  GDG+++ V ++CRIDTLDELDY++NGGIL YVL
Sbjct: 833 KGDELVEIDGL-STIKPRQTMIAKITYGDGTVKNVPIICRIDTLDELDYFKNGGILQYVL 891

Query: 902 RKLAA 906
           R LAA
Sbjct: 892 RDLAA 896


Lambda     K      H
   0.317    0.134    0.393 

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: 2305
Number of extensions: 90
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: 906
Length of database: 896
Length adjustment: 43
Effective length of query: 863
Effective length of database: 853
Effective search space:   736139
Effective search space used:   736139
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