GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Thioalkalivibrio paradoxus ARh 1

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_006747496.1 THITH_RS08500 aconitate hydratase AcnA

Query= SwissProt::O53166
         (943 letters)



>NCBI__GCF_000227685.2:WP_006747496.1
          Length = 916

 Score = 1066 bits (2757), Expect = 0.0
 Identities = 550/933 (58%), Positives = 676/933 (72%), Gaps = 36/933 (3%)

Query: 14  TLKVGEKSYQIYRLDAVPNTAKLPYSLKVLAENLLRNEDGSNITKDHIEAIANWDPKAEP 73
           TLK G +   I  +      A LPYSLK+L ENLLR EDG  + +  IEA+ +W+P+AEP
Sbjct: 11  TLKAGGRECAIVPITDDARAASLPYSLKILLENLLRFEDGRTVRRSDIEALLDWNPQAEP 70

Query: 74  SIEIQYTPARVVMQDFTGVPCIVDLATMREAIADLGGNPDKVNPLAPADLVIDHSVIADL 133
           + EI + PARV++QDFTGVP +VDLA MR+A+  LGG+P K+NP+ PA+LVIDHSV  D 
Sbjct: 71  AQEIAFRPARVLLQDFTGVPAVVDLAAMRDAMEALGGDPAKINPMQPAELVIDHSVQVDA 130

Query: 134 FGRADAFERNVEIEYQRNGERYQFLRWGQGAFDDFKVVPPGTGIVHQVNIEYLASVVMTR 193
            G  +A   N E+EY RN ERY FL+WGQ AF +FKVVPP TGIVHQVN+E+LA  V   
Sbjct: 131 HGNVNALNLNAELEYSRNRERYSFLKWGQQAFHNFKVVPPDTGIVHQVNLEFLARTVFLD 190

Query: 194 DGV-----AYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPVSMLIPRVVGFRL 248
           DG      AYPDT VGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQP+SMLIP+VVGFRL
Sbjct: 191 DGPDGRCRAYPDTLVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPISMLIPQVVGFRL 250

Query: 249 TGEIQPGVTATDVVLTVTEMLRQHGVVGKFVEFYGEGVAEVPLANRATLGNMSPEFGSTA 308
           TG +  G TATD+VL + EMLR+HGVVGKFVEF+GEG+A++PLA+RAT+ NM+PE+G+T 
Sbjct: 251 TGRLSEGATATDLVLVIVEMLRRHGVVGKFVEFFGEGLAQLPLADRATIANMAPEYGATC 310

Query: 309 AIFPIDEETIKYLRFTGRTPEQVALVEAYAKAQGMWHDPKHEP-EFSEYLELNLSDVVPS 367
            IFPID ET++YLR TGR P  V L+EAYA+AQG+W D    P  +++ LEL+L  V PS
Sbjct: 311 GIFPIDGETLEYLRLTGRDPGHVELIEAYARAQGLWRDDSAPPARYTDVLELDLGTVEPS 370

Query: 368 IAGPKRPQDRIALAQAKSTFREQIYHYVGNGSPDSPHDPHSKLDEVVEETFPASDPGQLT 427
           +AGP+RPQDR+ L +A     +++  ++G           S L E  E TF  S+P    
Sbjct: 371 LAGPRRPQDRLRLGEAG----KRVGEFIG-----------SMLKER-ESTF--SEP---- 408

Query: 428 FANDDVATDETVHSAAAHADGRVSNPVRVKSDELGE-FVLDHGAVVIAAITSCTNTSNPE 486
            A  +    E  H+A        + P R      GE FVLDHG +VIAAITSCTNTSNP 
Sbjct: 409 -AEAERFEAEGGHTAVGVEHQAEATPKRSNVTMNGEEFVLDHGDIVIAAITSCTNTSNPS 467

Query: 487 VMLGAALLARNAVEKGLTSKPWVKTTIAPGSQVVNDYYDRSGLWPYLEKLGFYLVGYGCT 546
           VMLGA L+AR A E+GL  KPWVKT++APGS+VV +Y   SGL   LE LGF++VGYGCT
Sbjct: 468 VMLGAGLVARKARERGLKVKPWVKTSLAPGSKVVTEYLQHSGLLDDLEALGFHVVGYGCT 527

Query: 547 TCIGNSGPLPEEISKAVNDNDLSVTAVLSGNRNFEGRINPDVKMNYLASPPLVIAYALAG 606
           TCIGNSGPLP+ IS+AV  +DL V++VLSGNRNFEGRI+ +V+MN+LASPPLV+AYALAG
Sbjct: 528 TCIGNSGPLPDPISEAVLKDDLIVSSVLSGNRNFEGRIHSEVRMNFLASPPLVVAYALAG 587

Query: 607 TMDFDFQTQPLGQDKDGKNVFLRDIWPSQQDVSDTIAAAINQEMFTRNYADVFKGDDRWR 666
           TM  D    P+GQD+ G+ V+L+D+WPS  ++   + A++  + FT  Y DV++G+DRW 
Sbjct: 588 TMATDLLNDPIGQDEQGQPVYLKDVWPSNAEIQAMVTASVTAKSFTEAYRDVYRGEDRWM 647

Query: 667 NLPTPSGNTFEWDPNSTYVRKPPYFEGMTAKPEPVGNISGARVLALLGDSVTTDHISPAG 726
            L  P G  FEW  +STYVR PPYF GMT  P P+  I  ARVLALLGDSVTTDHISPAG
Sbjct: 648 RLAAPEGERFEWTEDSTYVRNPPYFTGMTMTPAPLTEIRDARVLALLGDSVTTDHISPAG 707

Query: 727 AIKPGTPAARYLDEHGVDRKDYNSFGSRRGNHEVMIRGTFANIRLRNQLLDDVSGGYTRD 786
           AI+P +PA +YL   GV   D+NS+GSRRGNHEVM+RGTFAN+RLRN L     GG T  
Sbjct: 708 AIRPDSPAGKYLASQGVKTADFNSYGSRRGNHEVMMRGTFANVRLRNLLAPGTEGGVTLH 767

Query: 787 FTQPGGPQAFIYDAAQNYAAQHIPLVVFGGKEYGSGSSRDWAAKGTLLLGVRAVIAESFE 846
              P G Q  IYDAA  Y  +++PL+V  GKEYG+GSSRDWAAKGT+LLGVRAVI ESFE
Sbjct: 768 L--PAGEQMPIYDAAIRYQQENVPLIVIAGKEYGTGSSRDWAAKGTMLLGVRAVIVESFE 825

Query: 847 RIHRSNLIGMGVIPLQFPEGKSASSLGLDGTEVFDITGIDVLNDGKTPKTVCVQATKGDG 906
           RIHRSNLIGMGV+PLQF  G++A SLGL G E + I G+D   +G+  + V V+A + DG
Sbjct: 826 RIHRSNLIGMGVLPLQFLPGENAESLGLTGRETYSIEGLD---EGRAAE-VTVRARRDDG 881

Query: 907 ATIEFDAVVRIDTPGEADYYRNGGILQYVLRNI 939
           +   F A VRIDTP E DY+R+GGIL YVLR +
Sbjct: 882 SEHRFQARVRIDTPQEVDYFRHGGILPYVLRQL 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: 2299
Number of extensions: 88
Number of successful extensions: 6
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: 916
Length adjustment: 43
Effective length of query: 900
Effective length of database: 873
Effective search space:   785700
Effective search space used:   785700
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