GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Sinorhizobium medicae WSM419

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_011974570.1 SMED_RS01825 aconitate hydratase AcnA

Query= SwissProt::Q5SMF6
         (902 letters)



>NCBI__GCF_000017145.1:WP_011974570.1
          Length = 872

 Score =  763 bits (1969), Expect = 0.0
 Identities = 414/880 (47%), Positives = 560/880 (63%), Gaps = 33/880 (3%)

Query: 21  YDLQELERKGVAEVSRLPFSIRVMLESLLRN--EDGYQVTREDIEALARWRPDPGEINVP 78
           YD+ +L  +   ++  LP+  R++LE++LR   ED  +     I+ LA       E+ + 
Sbjct: 14  YDVIDLPAEVGHQLRSLPYIHRILLENVLRTAGEDAARAKAAIIDWLAT---GSSELEIQ 70

Query: 79  LKLARVILQDFTGVPAVVDLAAMRDAIKAKGGDPKRINPVVPADLVIDHSVQVDAFGTAY 138
               RV++ D T  PA+VD+A MR A+   G DP  +NPVVP D+  DHS+ VD FG + 
Sbjct: 71  FLPNRVMMHDTTCGPALVDIAGMRSALAEAGYDPALLNPVVPVDVSTDHSLAVDVFGHSA 130

Query: 139 AFFYNVEKEYERNRERYLLLKWAQNALENFRVVPPGTGIVHQVNIEYLTKVVMTGKRDGL 198
           +   N+++E+ERN ERY  +KWA N L  FRV PPGTGI+H +N+E L  VV T ++DG 
Sbjct: 131 SLELNMKREFERNAERYRFMKWATNTLTGFRVHPPGTGIMHTLNLERLATVVSTLEKDGR 190

Query: 199 TLAFPDSLVGTDSHTTMVNGLGVLGWGVGGIEAEAVMLGQPYYMLAPRVVGFKLYGELPE 258
             A PD+L+GTDSHT M+NG+GVL WGVGG+EAE+V  G P  +  P VVG +L G L +
Sbjct: 191 RWAAPDTLIGTDSHTPMINGIGVLAWGVGGLEAESVFFGMPVSLRVPDVVGVRLTGRLGD 250

Query: 259 GATATDLVLTVTEMLRKHGVVGKFVEFYGPGVAKLSTPDRATIANMAPEYGATMGFFPVD 318
           G  ATDL LTVT +LRK  +  K+VEFYGPGV+ L+  DR+ +ANM PE+G   G+FPVD
Sbjct: 251 GVLATDLALTVTHILRKIDLQDKYVEFYGPGVSLLTAGDRSVVANMTPEFGGNSGYFPVD 310

Query: 319 EETLNYLRQTGRPEELVELVEAYTKAVGLFRTPEAEEKVQYSEYLELDLSAVEPSLAGPK 378
             TL+YLR TGR  E VELVEA+TK VGL+  P  +EK +Y+  +E+DLSA+EPSLAGP 
Sbjct: 311 GRTLDYLRTTGRTSEQVELVEAFTKRVGLWFDP--DEKPRYTHVVEIDLSAIEPSLAGPT 368

Query: 379 RPQDRVPLKEVKKSFLAHLTKPVKERGFGLSEDQLQRKVLVKRRDEEFELTHGSVVIAAI 438
           RP DR+ + E   +                    ++R  +V       E   G+V IAAI
Sbjct: 369 RPHDRISVGETSAAI-----------------SSMKRDAVVSAHTS--EPNDGAVAIAAI 409

Query: 439 TSCTNTSNPSVMLGAGLLAKKAVEAGLDRKPWVKTSLAPGSKVVTDYLEMSGLMPFLEAL 498
           TSCTNTS+P +++ AGLLA+KA   GL   PWVKTSLAPGS     YL  SGL+  LEA+
Sbjct: 410 TSCTNTSDPRLVIAAGLLARKARALGLHPAPWVKTSLAPGSPTAERYLRRSGLLQDLEAV 469

Query: 499 GFHLVGYGCTTCIGNSGPLPEDIAKAVEEGNLVVAAVLSGNRNFEGRINPHVKANYLASP 558
           GF +VGYGCTTCIGNSGPL E IA A+++  ++  AVLSGNRNF GR++P ++A +LASP
Sbjct: 470 GFGIVGYGCTTCIGNSGPLTEPIAVAMKDRGILPVAVLSGNRNFPGRVHPQLEAGFLASP 529

Query: 559 MLVVAYALAGRMDIDFTTEPLGFDPNGKPIYLKDIWPSMEEIREAIRKTLDPELFKKEYS 618
            LVVA+ALAG ++++  T+ +G   +G+ + L  +WP+ +EI EA+    D   FK+ Y 
Sbjct: 530 PLVVAFALAGTVELNILTDVIGRSSDGQAVTLSMLWPTSQEIDEAVTLAADAMDFKRAYD 589

Query: 619 KVFEGDERWQALPAPTGELYQWDPESTYIQNPPFFEDLGERKVEDIRGARVLLVLGDSVT 678
           +  E  + W+ L APT  L+ WD  STYI+ PP F   G+  +     A  L+V+GD +T
Sbjct: 590 EA-EASKAWRELEAPTTTLFPWDETSTYIRRPP-FAGFGKGSLLGTYDAHPLIVVGDDIT 647

Query: 679 TDHISPAGAIPVKSPAGQYLISKGVKPEDFNSYGSRRGNHEVMMRGTFANIRIKNLMLDG 738
           TDHISPAGAI  +S  G+YL+  G  P D N + SRRGN E M+RG + N  ++N +   
Sbjct: 648 TDHISPAGAIRAQSETGRYLVELGEVPTDLNVHASRRGNWESMVRGLYTNRTVQNFLGVE 707

Query: 739 IEGGYAKKLPEGDVDFVYNVAMRYKAEGTPLLVIAGKEYGTGSSRDWAAKGTYLLGIRAV 798
           I  G     P G++  +++ A RY      ++++AG+ YG GSSRDWAAKG  LLG RAV
Sbjct: 708 IPPGSTIHAPSGELLPLWSAANRYAESKQSVVIVAGERYGMGSSRDWAAKGASLLGARAV 767

Query: 799 LAESFERIHRSNLVGMGVLPLEFLPGENRETLGLTGYEVYDI---LGLEDLKPRKLVDIV 855
           LA SFERIHRSNL+GMGVLP+    G   + L L   ++ +I    GL  + PR  +D+V
Sbjct: 768 LAVSFERIHRSNLIGMGVLPMRLPEGLGPDELALRSGDLIEIHADAGL--IAPRCPIDVV 825

Query: 856 ARREDGSEVRFQAIARLDTPVEVDYYKNGGILQTVLLNML 895
            RR DG   RF+A   ++T  EV+  K GGIL  +L N++
Sbjct: 826 IRRRDGEITRFRATTAIETVAEVEMLKAGGILPLMLKNLV 865


Lambda     K      H
   0.317    0.137    0.399 

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: 1903
Number of extensions: 79
Number of successful extensions: 7
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: 902
Length of database: 872
Length adjustment: 43
Effective length of query: 859
Effective length of database: 829
Effective search space:   712111
Effective search space used:   712111
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 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