GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Halomonas xinjiangensis TRM 0175

Align Aconitate hydratase A; ACN; Aconitase; (2R,3S)-2-methylisocitrate dehydratase; (2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate dehydratase; 2-methyl-cis-aconitate hydratase; Iron-responsive protein-like; IRP-like; RNA-binding protein; EC 4.2.1.3; EC 4.2.1.99 (characterized)
to candidate WP_043529276.1 JH15_RS08095 aconitate hydratase AcnA

Query= SwissProt::Q8ZP52
         (891 letters)



>NCBI__GCF_000759345.1:WP_043529276.1
          Length = 914

 Score = 1243 bits (3217), Expect = 0.0
 Identities = 622/903 (68%), Positives = 724/903 (80%), Gaps = 27/903 (2%)

Query: 12  TLQAKDKTYHYYSLPLAAKSLGDIARLPKSLKVLLENLLRWQDGESVTDEDIQALAGWLK 71
           +L   ++ YHYYSLP AA++LGDI RLP +LK+LLEN LR+ D ESV+ ED+QAL  W +
Sbjct: 12  SLTVGEREYHYYSLPKAAEALGDIQRLPVTLKILLENQLRFADDESVSREDMQALVDWQQ 71

Query: 72  NAHADREIAWRPARVLMQDFTGVPAVVDLAAMREAVKRLGGDTSKVNPLSPVDLVIDHSV 131
            A + REI +RPARVLMQDFTGVP VVDLA+MR AV++LG D S++NPLSPVDLVIDHSV
Sbjct: 72  EARSTREIGYRPARVLMQDFTGVPGVVDLASMRAAVEKLGEDPSRINPLSPVDLVIDHSV 131

Query: 132 TVDHFGDDDAFEENVRLEMERNHERYMFLKWGKQAFSRFSVVPPGTGICHQVNLEYLGKA 191
            VD +GD  AF +NV +EM+RN ERY FL+WG+ AF  F VVPPGTGICHQVNLEYLGK 
Sbjct: 132 MVDKYGDPSAFRDNVAIEMDRNRERYEFLRWGQDAFDNFRVVPPGTGICHQVNLEYLGKT 191

Query: 192 VWSELQDGEWIAYPDSLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLIPDVVG 251
           VW + +DG+  AYPD+LVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLIP+VVG
Sbjct: 192 VWVKEEDGKSFAYPDTLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLIPEVVG 251

Query: 252 FKLTGKLREGITATDLVLTVTQMLRKHGVVGKFVEFYGDGLDSLPLADRATIANMSPEYG 311
           FKLTGKLREGITATDLVLTVTQMLR+ GVVGKFVEFYGDGLD LPLADRATIANM+PEYG
Sbjct: 252 FKLTGKLREGITATDLVLTVTQMLRQKGVVGKFVEFYGDGLDDLPLADRATIANMAPEYG 311

Query: 312 ATCGFFPIDAITLEYMRLSGRSDDLVELVETYAKAQGMWRNPGDEPVFTSTLELDMGDVE 371
           ATCGFFP+D  TL Y+RL+GRSD+ V LVE Y K Q +WR PG EPVF+ TL+LDMGDVE
Sbjct: 312 ATCGFFPVDDETLNYLRLTGRSDEEVALVEAYCKEQDLWRKPGAEPVFSDTLQLDMGDVE 371

Query: 372 ASLAGPKRPQDRVALGDVPKAF-------AASA-------------ELELNTAQR----D 407
           ASLAGPKRPQDRVAL D+   F       AA A             ++ + T +     D
Sbjct: 372 ASLAGPKRPQDRVALSDMKSTFENLMGDDAAEASATARGKFDSEGGQMPVGTHEHFEHHD 431

Query: 408 RQPVDYTMNGQPYQLPDGAVVIAAITSCTNTSNPSVLMAAGLLAKKAVTLGLKRQPWVKA 467
            Q VD  + G  ++L  GAVVIAAITSCTNTSNPSV+MAAGLLA+KAV  GL  +PWVK 
Sbjct: 432 SQDVD--VEGSTFKLNPGAVVIAAITSCTNTSNPSVMMAAGLLARKAVEKGLDTKPWVKT 489

Query: 468 SLAPGSKVVSDYLAQAKLTPYLDELGFNLVGYGCTTCIGNSGPLPEPIETAIKKGDLTVG 527
           SLAPGSKVV+DYLA       L+ LGFNLVGYGCTTCIGNSGPL  PIE AI+ GDLTV 
Sbjct: 490 SLAPGSKVVTDYLAAGGFQDDLNALGFNLVGYGCTTCIGNSGPLLPPIEKAIEDGDLTVA 549

Query: 528 AVLSGNRNFEGRIHPLVKTNWLASPPLVVAYALAGNMNINLATDPLGYDRKGDPVYLKDI 587
           +VLSGNRNFEGR+HPLVKTNWLASPPLVVAYALAGN+ ++++ +PLG  + G PVYL+DI
Sbjct: 550 SVLSGNRNFEGRVHPLVKTNWLASPPLVVAYALAGNVRLDISKEPLGEGKDGKPVYLQDI 609

Query: 588 WPSAQEIARAVELVSSDMFRKEYAEVFEGTEEWKSIQVESSDTYGWQSDSTYIRLSPFFD 647
           WPS  EIA AVE V ++M+RKEYAEVFEG E WK+I V  S  Y W  DSTYI+  PFF+
Sbjct: 610 WPSQAEIAEAVEKVRTEMYRKEYAEVFEGDEVWKAIDVPQSQVYQWSEDSTYIQHPPFFE 669

Query: 648 EMQAQPAPVKDIHGARILAMLGDSVTTDHISPAGSIKPDSPAGRYLQNHGVERKDFNSYG 707
            M  +P P++D+  AR+LAMLGDSVTTDHISPAG+IKPDSPAGRYLQ HGV+  DFNSYG
Sbjct: 670 GMGREPEPLQDVENARVLAMLGDSVTTDHISPAGAIKPDSPAGRYLQEHGVKPMDFNSYG 729

Query: 708 SRRGNHEVMMRGTFANIRIRNEMLPGVEGGMTRHLPGTEAMSIYDAAMLYQQEKTPLAVI 767
           SRRGNHEVMMRGTFAN+RIRNEML GVEGG TRH+P  E M+IYDAAM Y +E  PL VI
Sbjct: 730 SRRGNHEVMMRGTFANVRIRNEMLDGVEGGYTRHVPSDEQMAIYDAAMKYAEEGRPLVVI 789

Query: 768 AGKEYGSGSSRDWAAKGPRLLGIRVVIAESFERIHRSNLIGMGILPLEFPQGVTRKTLGL 827
           AGKEYG+GSSRDWAAKG RLLG+R V+AES+ERIHRSNLIGMG++PL+FP+G  RK+LGL
Sbjct: 790 AGKEYGTGSSRDWAAKGTRLLGVRAVLAESYERIHRSNLIGMGVVPLQFPEGEDRKSLGL 849

Query: 828 TGEEVIDIADLQNLRPGATIPVTLTRSDGSKETVPCRCRIDTATELTYYQNDGILHYVIR 887
           TG+E + I  + +L PG  + VT+ +SD  ++ +   CRIDTA EL YY++ GILHYV+R
Sbjct: 850 TGDEEVSIDGIADLTPGGQVNVTI-KSDKGEKKIEALCRIDTANELEYYRHGGILHYVLR 908

Query: 888 NML 890
            M+
Sbjct: 909 KMI 911


Lambda     K      H
   0.317    0.135    0.401 

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: 2309
Number of extensions: 92
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: 891
Length of database: 914
Length adjustment: 43
Effective length of query: 848
Effective length of database: 871
Effective search space:   738608
Effective search space used:   738608
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 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