GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Stenotrophomonas chelatiphaga DSM 21508

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_057687523.1 ABB28_RS16850 aconitate hydratase AcnA

Query= SwissProt::O53166
         (943 letters)



>NCBI__GCF_001431535.1:WP_057687523.1
          Length = 917

 Score = 1103 bits (2852), Expect = 0.0
 Identities = 558/944 (59%), Positives = 694/944 (73%), Gaps = 43/944 (4%)

Query: 7   NSFGAHDTLKVGEKSYQIYRLDAVP---NTAKLPYSLKVLAENLLRNEDGS-NITKDHIE 62
           +SF     L VG K Y  + L  +    + + LPYS+K+L ENLLR+EDG   + KDHIE
Sbjct: 3   DSFSTRSQLDVGGKRYDYFSLPKLGQRFDISHLPYSMKILLENLLRHEDGGVTVGKDHIE 62

Query: 63  AIANWDPKAEPSIEIQYTPARVVMQDFTGVPCIVDLATMREAIADLGGNPDKVNPLAPAD 122
           A+A WDPKAEP IEI + PARVV+QDFTGVPC+VDLA MR+A+  LGG+P+++NP  P++
Sbjct: 63  AVATWDPKAEPEIEIAFMPARVVLQDFTGVPCVVDLAAMRDAVVKLGGSPEQINPQIPSE 122

Query: 123 LVIDHSVIADLFGRADAFERNVEIEYQRNGERYQFLRWGQGAFDDFKVVPPGTGIVHQVN 182
           LVIDHSV  D+FG+ +A + N +IE+QRN ERY FLRWGQ AFD+FKVVPP TGIVHQVN
Sbjct: 123 LVIDHSVQVDVFGKPEALDLNGKIEFQRNQERYGFLRWGQKAFDNFKVVPPNTGIVHQVN 182

Query: 183 IEYLASVVMT--RDG--VAYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPVSM 238
           +E LA VVM   +DG  VAYPDT  GTDSHTTM+NG+GVLGWGVGGIEAEAAMLGQP SM
Sbjct: 183 LENLARVVMAVDKDGTQVAYPDTVFGTDSHTTMINGIGVLGWGVGGIEAEAAMLGQPSSM 242

Query: 239 LIPRVVGFRLTGEIQPGVTATDVVLTVTEMLRQHGVVGKFVEFYGEGVAEVPLANRATLG 298
           LIP+VVGF+LTG++  G TATD+VLTVT+MLR+HGVVGKFVEF+GEG+  +PLA+RAT+G
Sbjct: 243 LIPQVVGFKLTGQMPEGATATDLVLTVTQMLRKHGVVGKFVEFFGEGLQHLPLADRATIG 302

Query: 299 NMSPEFGSTAAIFPIDEETIKYLRFTGRTPEQVALVEAYAKAQGMWHDPKH-EPEFSEYL 357
           NM+PE+G+T  IFPID E++ YLR +GR  EQ+ALVEAYAKAQG+WHD      ++S  L
Sbjct: 303 NMAPEYGATCGIFPIDHESLNYLRLSGRPEEQIALVEAYAKAQGLWHDADTAHAQYSATL 362

Query: 358 ELNLSDVVPSIAGPKRPQDRIALAQAKSTFREQIYHYVGNGSPDSPHDPHSKLDEVVEET 417
           EL++  V PS+AGPKRPQDR+ L   ++ +RE +     N              +V   T
Sbjct: 363 ELDMGTVKPSLAGPKRPQDRVLLEDVQANYREALVGLTTNRDKK----------DVDVST 412

Query: 418 FPASDPGQLTFANDDVATDETVHSAAAHADGRVSNPVRVKSDELGEFVLDHGAVVIAAIT 477
           F  ++ G     N+ +A  +    A    DG+              F L  GAVVIAAIT
Sbjct: 413 F-VNEGGGTAVGNEQLAKGQ----ADVELDGKA-------------FRLKDGAVVIAAIT 454

Query: 478 SCTNTSNPEVMLGAALLARNAVEKGLTSKPWVKTTIAPGSQVVNDYYDRSGLWPYLEKLG 537
           SCTNTSNP VM+GA LLARNA  +GL  +PWVKT++ PGS+VV DY  ++G+   LEKLG
Sbjct: 455 SCTNTSNPAVMIGAGLLARNAAARGLNRQPWVKTSLGPGSRVVTDYLSKAGVLTELEKLG 514

Query: 538 FYLVGYGCTTCIGNSGPLPEEISKAVNDNDLSVTAVLSGNRNFEGRINPDVKMNYLASPP 597
           FY+VGYGCTTCIGNSGPLP E+S  +   DL VT+VLSGNRNFEGR++P+VKMNYLASPP
Sbjct: 515 FYVVGYGCTTCIGNSGPLPAEVSAGIALGDLVVTSVLSGNRNFEGRVHPEVKMNYLASPP 574

Query: 598 LVIAYALAGTMDFDFQTQPLGQDKDGKNVFLRDIWPSQQDVSDTIAAAINQEMFTRNYAD 657
           LV+AYA+AGT D D  T+PLG   DG+ V+LRDIWPS +++ D IAA +  EMF +NYAD
Sbjct: 575 LVVAYAIAGTTDIDLTTEPLGTGSDGQPVYLRDIWPSNKEIGDVIAATLGPEMFKQNYAD 634

Query: 658 VFKGDDRWRNLPTPSGNTFEWDPNSTYVRKPPYFEGMTAKPEPVGNISGARVLALLGDSV 717
           VFKGD RW  + +P G+ +EWD  STY++ PPYF+GMT +   + ++ GARV+ L GDS+
Sbjct: 635 VFKGDSRWNTIASPDGDLYEWDDGSTYIKNPPYFDGMTMQVGSIDDVHGARVMGLFGDSI 694

Query: 718 TTDHISPAGAIKPGTPAARYLDEHGVDRKDYNSFGSRRGNHEVMIRGTFANIRLRNQLLD 777
           TTDHISPAG IK  +PA R+L E GV   D+NS+GSRRGN +VM+RGTFANIR++N +  
Sbjct: 695 TTDHISPAGNIKKESPAGRFLQERGVQPADFNSYGSRRGNDDVMVRGTFANIRIKNLMFG 754

Query: 778 DVSGGYTRDFTQPGG--PQAFIYDAAQNYAAQHIPLVVFGGKEYGSGSSRDWAAKGTLLL 835
              GG T  +   GG   +  IYDAA  Y A  +PLVV  GKEYG+GSSRDWAAKGTLLL
Sbjct: 755 GEEGGNTLYYPASGGEPEKLAIYDAAIKYKADGVPLVVLAGKEYGTGSSRDWAAKGTLLL 814

Query: 836 GVRAVIAESFERIHRSNLIGMGVIPLQFPEGKSASSLGLDGTEVFDITGIDVLNDGKTPK 895
           GV+AVIAESFERIHRSNL+GMGV+PLQF  G++A SLGLDG+EVFDITG   L DG + K
Sbjct: 815 GVKAVIAESFERIHRSNLVGMGVLPLQFRNGENAQSLGLDGSEVFDITG---LKDGAS-K 870

Query: 896 TVCVQATKGDGATIEFDAVVRIDTPGEADYYRNGGILQYVLRNI 939
              V A K DG  + F+A V + TP E +Y+R+GG+LQYVLR +
Sbjct: 871 RATVAAKKADGTVVTFEASVMLLTPKEVEYFRHGGLLQYVLRQL 914


Lambda     K      H
   0.316    0.136    0.403 

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: 2508
Number of extensions: 133
Number of successful extensions: 8
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: 943
Length of database: 917
Length adjustment: 43
Effective length of query: 900
Effective length of database: 874
Effective search space:   786600
Effective search space used:   786600
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: 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