GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Thiohalospira halophila HL 3

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_093427176.1 BM272_RS02610 aconitate hydratase AcnA

Query= SwissProt::O53166
         (943 letters)



>NCBI__GCF_900112605.1:WP_093427176.1
          Length = 914

 Score = 1067 bits (2760), Expect = 0.0
 Identities = 543/942 (57%), Positives = 681/942 (72%), Gaps = 41/942 (4%)

Query: 7   NSFGAHDTLKVGEKSYQIYRLDAVPNTAKLPYSLKVLAENLLRNEDGSNITKDHIEAIAN 66
           +SF A   L+ G   Y+  RLDAVP + +LPYSLK+L ENLLR+EDG  +T + I+ +AN
Sbjct: 3   DSFQARAELEAGGNRYRYVRLDAVPGSERLPYSLKILLENLLRHEDGRTVTAEDIQRLAN 62

Query: 67  WDPKAEPSIEIQYTPARVVMQDFTGVPCIVDLATMREAIADLGGNPDKVNPLAPADLVID 126
           WDP+AEP+ EI + PARV+MQDFTGVP +VDLA MR+A+A+LGG+P+ +NPL PA+LVID
Sbjct: 63  WDPQAEPAHEIAFRPARVLMQDFTGVPAVVDLAAMRDAMAELGGDPEHINPLQPAELVID 122

Query: 127 HSVIADLFGRADAFERNVEIEYQRNGERYQFLRWGQGAFDDFKVVPPGTGIVHQVNIEYL 186
           HSV  D +G  +A+  N  +EYQRN ERY FL+WGQG+F +FK VPPG GIVHQ+N+E+L
Sbjct: 123 HSVQVDHYGNGEAYGLNEALEYQRNRERYTFLKWGQGSFANFKAVPPGKGIVHQINLEHL 182

Query: 187 ASVVMTRDGV-----AYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPVSMLIP 241
             VV   +G      A+PDT VGTDSHT M+NGLGVLGWGVGGIEAEAAMLGQP+SML+P
Sbjct: 183 GRVVFGAEGPDGAQWAWPDTLVGTDSHTPMINGLGVLGWGVGGIEAEAAMLGQPISMLVP 242

Query: 242 RVVGFRLTGEIQPGVTATDVVLTVTEMLRQHGVVGKFVEFYGEGVAEVPLANRATLGNMS 301
           +VVGFRLTG++  G TATD+VLT+ E LR HGVVGKFVEF+G+G+ E+P+A+RAT+ NM+
Sbjct: 243 QVVGFRLTGQLPEGATATDLVLTIVEQLRAHGVVGKFVEFFGDGLDELPIADRATIANMA 302

Query: 302 PEFGSTAAIFPIDEETIKYLRFTGRTPEQVALVEAYAKAQGMWHDP-KHEPEFSEYLELN 360
           PE+G+T  IFP+D  T+ YLR TGR+ +QVA VEAYA+AQG++ +    E  ++  +EL+
Sbjct: 303 PEYGATCGIFPVDTATLDYLRLTGRSEDQVARVEAYARAQGLFRESGAPEAAYTSVVELD 362

Query: 361 LSDVVPSIAGPKRPQDRIALAQAKSTFREQIYHYVGNGSPDSPHDPHSKLDEVVEET--F 418
           L+ + PS+AGP+RPQDRIAL+QA+   RE                    LD ++ E    
Sbjct: 363 LATIEPSLAGPRRPQDRIALSQARRPIRES-------------------LDGILSERGMV 403

Query: 419 PASDPGQLTFANDDVATDETVHSAAAHADGRVSNPVRVKSDELGE-FVLDHGAVVIAAIT 477
           P  D     FA +   T   V     H         +V+ +  GE F LD G VVIAAIT
Sbjct: 404 PREDRETERFAAEGGHTAPGVEHQGDHRG-------KVRVERNGESFYLDDGMVVIAAIT 456

Query: 478 SCTNTSNPEVMLGAALLARNAVEKGLTSKPWVKTTIAPGSQVVNDYYDRSGLWPYLEKLG 537
           SCTNTSNP VMLGA LLA+ A+E+GL  KPWVKT++ PGS+VV DY + +GL   LE LG
Sbjct: 457 SCTNTSNPSVMLGAGLLAKKALERGLQVKPWVKTSLGPGSRVVTDYLEHAGLLDDLEGLG 516

Query: 538 FYLVGYGCTTCIGNSGPLPEEISKAVNDNDLSVTAVLSGNRNFEGRINPDVKMNYLASPP 597
           F +VGYGCTTCIGNSGPL E IS A+ ++DL V ++LSGNRNFEGRI+ +V+MNYLASPP
Sbjct: 517 FDVVGYGCTTCIGNSGPLDESISHAIREDDLVVCSILSGNRNFEGRIHSEVRMNYLASPP 576

Query: 598 LVIAYALAGTMDFDFQTQPLGQDKDGKNVFLRDIWPSQQDVSDTIAAAINQEMFTRNYAD 657
           LV+AYALAG MD D     LG D DG  V+LRDIWPSQ ++   +   +  + F + YAD
Sbjct: 577 LVVAYALAGRMDIDPYNDALGTDADGNAVYLRDIWPSQAEIQALVRDHVRADAFEQAYAD 636

Query: 658 VFKGDDRWRNLPTPSGNTFEWDPNSTYVRKPPYFEGMTAKPEPVGNISGARVLALLGDSV 717
           VF G +RW  L  P G  ++W  +STY+R+PP+FEG+  +PEPVG+I+GAR LA++GDSV
Sbjct: 637 VFAGGERWEALTAPGGRLYDWAEDSTYIRRPPFFEGIQPEPEPVGDITGARALAVVGDSV 696

Query: 718 TTDHISPAGAIKPGTPAARYLDEHGVDRKDYNSFGSRRGNHEVMIRGTFANIRLRNQLLD 777
           TTDHISPAG+I   +PA  YL E+GV+  ++NS+G+RRGNHEVM+RGTFAN R RN+L  
Sbjct: 697 TTDHISPAGSIAADSPAGHYLRENGVEPAEFNSYGARRGNHEVMMRGTFANPRFRNRLAP 756

Query: 778 DVSGGYTRDFTQPGGPQAFIYDAAQNYAAQHIPLVVFGGKEYGSGSSRDWAAKGTLLLGV 837
           D  GG+T    QP G    IYDAA  YA +  PLVV  GKEYGSGSSRDWAAKG  LLGV
Sbjct: 757 DTEGGWTAH--QPSGKVMPIYDAAMRYAEEGTPLVVLAGKEYGSGSSRDWAAKGPRLLGV 814

Query: 838 RAVIAESFERIHRSNLIGMGVIPLQFPEGKSASSLGLDGTEVFDITGIDVLNDGKTPKTV 897
           RAVIAES+ERIHRSNL+GMG++PLQF +G +A SLGLDGTE F + G   L DG   + V
Sbjct: 815 RAVIAESYERIHRSNLVGMGILPLQFRDGDTADSLGLDGTETFALAG---LGDGSADQ-V 870

Query: 898 CVQATKGDGATIEFDAVVRIDTPGEADYYRNGGILQYVLRNI 939
            V AT  DG    F A VRIDTP E +YYR+GGIL YVLR +
Sbjct: 871 TVTATTADGGETTFTARVRIDTPQEVEYYRHGGILPYVLRQL 912


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: 2554
Number of extensions: 130
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: 914
Length adjustment: 43
Effective length of query: 900
Effective length of database: 871
Effective search space:   783900
Effective search space used:   783900
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.

Links

Downloads

Related tools

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