GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Pseudarthrobacter sulfonivorans Ar51

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_058929322.1 AU252_RS02190 aconitate hydratase AcnA

Query= SwissProt::O53166
         (943 letters)



>NCBI__GCF_001484605.1:WP_058929322.1
          Length = 936

 Score = 1365 bits (3533), Expect = 0.0
 Identities = 676/941 (71%), Positives = 780/941 (82%), Gaps = 16/941 (1%)

Query: 5   SVNSFGAHDTLKVGEKSYQIYRLDAVPNTAKLPYSLKVLAENLLRNEDGSNITKDHIEAI 64
           +V+SFG+   L V    Y+I+RL++V     LP+SLKVL ENLLR EDG+NIT DH+ A+
Sbjct: 3   TVDSFGSKGKLNVAGTEYEIFRLNSVEGAENLPFSLKVLLENLLRTEDGANITADHVRAL 62

Query: 65  ANWDPKAEPSIEIQYTPARVVMQDFTGVPCIVDLATMREAIADLGGNPDKVNPLAPADLV 124
           A WDP A+P+ EIQ+TPARV+MQDFTGVPC+VDLATMREA+ +LGG+P +VNPLAPA++V
Sbjct: 63  AGWDPDAQPNTEIQFTPARVIMQDFTGVPCVVDLATMREAVKELGGDPKRVNPLAPAEMV 122

Query: 125 IDHSVIADLFGRADAFERNVEIEYQRNGERYQFLRWGQGAFDDFKVVPPGTGIVHQVNIE 184
           IDHSV  D FG + A ERN+EIEYQRNGERYQFLRWGQ AFDDFKVVPPGTGIVHQVNIE
Sbjct: 123 IDHSVQIDAFGNSGALERNMEIEYQRNGERYQFLRWGQTAFDDFKVVPPGTGIVHQVNIE 182

Query: 185 YLASVVMTR--DGV--AYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPVSMLI 240
           YLA  VMTR  DGV  AYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPVSMLI
Sbjct: 183 YLARTVMTREIDGVLRAYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPVSMLI 242

Query: 241 PRVVGFRLTGEIQPGVTATDVVLTVTEMLRQHGVVGKFVEFYGEGVAEVPLANRATLGNM 300
           PRVVGF+LTG I  G TATDVVLT+TE LR+HGVVGKFVEFYGEGVA VPLANRAT+GNM
Sbjct: 243 PRVVGFKLTGSIPAGATATDVVLTITEQLRKHGVVGKFVEFYGEGVAAVPLANRATIGNM 302

Query: 301 SPEFGSTAAIFPIDEETIKYLRFTGRTPEQVALVEAYAKAQGMWHDPKHEPEFSEYLELN 360
           SPEFGSTAA+FPID+ T+ YLR TGR+ E VALVE+YAK QG+WHD   E +FSEYLEL+
Sbjct: 303 SPEFGSTAAMFPIDDVTLDYLRLTGRSDENVALVESYAKEQGLWHDASREIKFSEYLELD 362

Query: 361 LSDVVPSIAGPKRPQDRIALAQAKSTFREQIYHYVG--NGSPDSPHDPHSKLDEVVEETF 418
           LS VVPSI+GPKRPQDRI L  AK  FR+ I++YV   +GS          +DE ++E+F
Sbjct: 363 LSTVVPSISGPKRPQDRIELTDAKEQFRKDIHNYVAIEDGS----------VDESLDESF 412

Query: 419 PASDPGQLTFANDDVATDETVHSAAAHADGRVSNPVRVKSDELGEFVLDHGAVVIAAITS 478
           PASD    T A+        V SAA  A GR SNPV +K+++  EF LDHGAV IA+ITS
Sbjct: 413 PASDAPSFTHADSHTTETSRVVSAANGAHGRPSNPVHIKTEDGREFELDHGAVSIASITS 472

Query: 479 CTNTSNPEVMLGAALLARNAVEKGLTSKPWVKTTIAPGSQVVNDYYDRSGLWPYLEKLGF 538
           CTNTSNP VML AALLARNAV+KGLTSKPWVKT++APGS+VV DYY++SGL PYLEKLGF
Sbjct: 473 CTNTSNPSVMLAAALLARNAVDKGLTSKPWVKTSVAPGSKVVTDYYNKSGLTPYLEKLGF 532

Query: 539 YLVGYGCTTCIGNSGPLPEEISKAVNDNDLSVTAVLSGNRNFEGRINPDVKMNYLASPPL 598
           Y+VGYGC TCIGNSGPL  EIS+A+  NDLSVTAVLSGNRNFEGRINPDVKMNYLASPPL
Sbjct: 533 YIVGYGCATCIGNSGPLDAEISEAIQANDLSVTAVLSGNRNFEGRINPDVKMNYLASPPL 592

Query: 599 VIAYALAGTMDFDFQTQPLGQDKDGKNVFLRDIWPSQQDVSDTIAAAINQEMFTRNYADV 658
           VIAYALAG+MDFDF T  LG+D+ G +VFL+DIWP+  +V   I ++I+++MF R Y  V
Sbjct: 593 VIAYALAGSMDFDFDTDSLGKDEAGNDVFLKDIWPNPVEVQQVIDSSIDKDMFARGYEGV 652

Query: 659 FKGDDRWRNLPTPSGNTFEWDPNSTYVRKPPYFEGMTAKPEPVGNISGARVLALLGDSVT 718
           F GD RW+ L TP+G+TF WDPNSTYVRKPPYF+G+ A+PEPV +ISGARVL  LGDSVT
Sbjct: 653 FDGDARWKALDTPAGDTFAWDPNSTYVRKPPYFDGIKAQPEPVQDISGARVLLKLGDSVT 712

Query: 719 TDHISPAGAIKPGTPAARYLDEHGVDRKDYNSFGSRRGNHEVMIRGTFANIRLRNQLLDD 778
           TDHISPAG+ K  TPA +YL  +GV+RKD+NS+GSRRGNHEVMIRGTFANIR++NQ+LD 
Sbjct: 713 TDHISPAGSFKSDTPAGQYLLANGVERKDFNSYGSRRGNHEVMIRGTFANIRIKNQILDG 772

Query: 779 VSGGYTRDFTQPGGPQAFIYDAAQNYAAQHIPLVVFGGKEYGSGSSRDWAAKGTLLLGVR 838
           V GG+TRDFTQ  GPQA++YDAAQNY A   PLVV  GKEYGSGSSRDWAAKGT LLGV+
Sbjct: 773 VEGGFTRDFTQADGPQAYVYDAAQNYQAAGTPLVVLAGKEYGSGSSRDWAAKGTALLGVK 832

Query: 839 AVIAESFERIHRSNLIGMGVIPLQFPEGKSASSLGLDGTEVFDITGIDVLNDGKTPKTVC 898
           AV+AES+ERIHRSNLIGMGV+PLQFP G+SA++LGL GTE F + G+  LN+G TPKT+ 
Sbjct: 833 AVVAESYERIHRSNLIGMGVLPLQFPAGESAATLGLTGTETFAVEGVTALNEGTTPKTLK 892

Query: 899 VQATKGDGATIEFDAVVRIDTPGEADYYRNGGILQYVLRNI 939
           V AT  DG+   FDAV+RIDTPGEADYYRNGGILQYVLR I
Sbjct: 893 VTATAEDGSAKSFDAVLRIDTPGEADYYRNGGILQYVLRQI 933


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: 2570
Number of extensions: 99
Number of successful extensions: 3
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: 936
Length adjustment: 44
Effective length of query: 899
Effective length of database: 892
Effective search space:   801908
Effective search space used:   801908
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 Apr 09 2024. 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