GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Halomonas stevensii S18214

Align Aconitate hydratase A; ACN; Aconitase; (2R,3S)-2-methylisocitrate dehydratase; (2S,3R)-3-hydroxybutane-1,2,3-tricarboxylate dehydratase; IP210; Iron-responsive protein-like; IRP-like; Major iron-containing protein; MICP; Probable 2-methyl-cis-aconitate hydratase; RNA-binding protein; EC 4.2.1.3; EC 4.2.1.99 (characterized)
to candidate WP_016916040.1 HSS18214_RS0114705 aconitate hydratase AcnA

Query= SwissProt::P37032
         (891 letters)



>NCBI__GCF_000275725.1:WP_016916040.1
          Length = 915

 Score = 1169 bits (3025), Expect = 0.0
 Identities = 594/910 (65%), Positives = 700/910 (76%), Gaps = 33/910 (3%)

Query: 9   STKSQLTVDGKTYNYYSLKEAENKHFKGINRLPYSLKVLLENLLRFEDGNTVTTKDIKAI 68
           ST   LT   + Y+YYSL +A       I+RLP +LK+LLEN LRF D  +V   D++A+
Sbjct: 6   STLHTLTAGSQEYHYYSLPKAAET-LGNIDRLPKTLKILLENQLRFADDESVEQADMQAL 64

Query: 69  ADWLHNKTSQHEIAFRPTRVLMQDFTGVPAVVDLAAMRTAIVKMGGNADKISPLSPVDLV 128
            DW +   S  EI +RP RVLMQDFTGVP VVDLA+MR A+  +G +  +I+PLSPVDLV
Sbjct: 65  VDWQNEGQSSREIGYRPARVLMQDFTGVPGVVDLASMRAAVESLGEDPARINPLSPVDLV 124

Query: 129 IDHSVMVDKFASADALEVNTKIEIERNKERYEFLRWGQKAFSNFQVVPPGTGICHQVNLE 188
           IDHSVMVDKF +  A + N  IE++RN ERYEFLRWGQKAF NF VVPPGTGICHQVNLE
Sbjct: 125 IDHSVMVDKFGTPTAFQENVDIEMQRNGERYEFLRWGQKAFDNFSVVPPGTGICHQVNLE 184

Query: 189 YLGKTVWNSENDGQLYAYPDTLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLI 248
           YLG+TVW  + DG+ +AYPDTLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLI
Sbjct: 185 YLGRTVWTKQEDGKTFAYPDTLVGTDSHTTMINGLGVLGWGVGGIEAEAAMLGQPVSMLI 244

Query: 249 PEVIGFKLSGKLKEGITATDLVLTVTQMLRKKGVVGKFVEFYGPGLNDLPLADRATISNM 308
           PEVIGFKL+GKL+EGITATDLVLTVT+MLRKKGVVGKFVEFYG GL DLPLADRATI+NM
Sbjct: 245 PEVIGFKLTGKLQEGITATDLVLTVTEMLRKKGVVGKFVEFYGDGLKDLPLADRATIANM 304

Query: 309 APEYGATCGFFPVDKETIKYLELTGRDKHTIALVEAYAKAQGMWYDKDNEEPVFTDSLHL 368
           APEYGATCGFFPVD ET+ YL LTGR+   +ALVEAY+KAQG+W +   +EP+FTD+L L
Sbjct: 305 APEYGATCGFFPVDDETLNYLRLTGREDELVALVEAYSKAQGLWRE-PGDEPIFTDTLSL 363

Query: 369 DLGSVEPSLAGPKRPQDKVNLSSLPVEFNNFLIEVGK---------------------EK 407
           D+ SVE SLAGPKRPQD+V+L ++P  F + + E GK                     ++
Sbjct: 364 DMSSVEASLAGPKRPQDRVSLKNMPKAFASVMEEDGKSYPATETGKLSSEGGQTAVGIDR 423

Query: 408 EKEKTF------AVK--NKDFQMKHGHVVIAAITSCTNTSNPSVLMAAGLVAKKAIEKGL 459
             E+ F      AVK   +DF +  G VVIAAITSCTNTSNPSV+MAAGL+A+ A +KGL
Sbjct: 424 SFERAFQHNDSQAVKMGEQDFNLDPGAVVIAAITSCTNTSNPSVMMAAGLLARNARQKGL 483

Query: 460 QRKPWVKSSLAPGSKVVTDYLRHAGLQTYLDQLGFNLVGYGCTTCIGNSGPLPDDISHCV 519
             KPWVK+SLAPGSKVVTDYL  A L   LD LGFNLVGYGCTTCIGNSGPLPD I   +
Sbjct: 484 ATKPWVKTSLAPGSKVVTDYLAAAELNDDLDALGFNLVGYGCTTCIGNSGPLPDAIEKAI 543

Query: 520 AEHDLVVSSVLSGNRNFEGRVHPQVRANWLASPPLVVAYALCGTTCSDLSREPIGQDKEG 579
            + DL V+SVLSGNRNFEGRVHP V+ NWLASPPLVVAYAL G    +LS +P+G+D +G
Sbjct: 544 QQGDLAVASVLSGNRNFEGRVHPLVKTNWLASPPLVVAYALAGNVQCNLSTDPLGEDSDG 603

Query: 580 NDVYLKDIWPSNEEIAAEVAKVSGTMFRKEYAEVFKGDAHWQAIQTSSGQTYEWNPDSTY 639
           N VYLKDIWPS  +IA  V KV+  MFRKEY+ VF+GD  WQ+I+      YEW P STY
Sbjct: 604 NPVYLKDIWPSQADIANAVQKVNTEMFRKEYSAVFEGDETWQSIKVPESNVYEW-PSSTY 662

Query: 640 IQHPPFFENLSLKPEPLKPIKQAYVLALFGDSITTDHISPAGSIKASSPAGLYLKSKGVD 699
           IQHPPFF+ +  +P+ ++ I+ A VLA+ GDS+TTDHISPAGSIK  SPAG YL+  GV 
Sbjct: 663 IQHPPFFKGMQREPDAIEDIQSARVLAILGDSVTTDHISPAGSIKPDSPAGRYLQEHGVK 722

Query: 700 EKDFNSYGSRRGNHEVMMRGTFANIRIRNEMTPGQEGGVTRYVPTGETMSIYDAAMRYQE 759
             DFNSYGSRRGNHEVMMRGTFAN+RI+NEM  G  GG TR+VP+GE MSIYDAAM+Y+E
Sbjct: 723 PVDFNSYGSRRGNHEVMMRGTFANVRIKNEMLDGVVGGETRHVPSGEQMSIYDAAMKYKE 782

Query: 760 NQQDLVIIAGKEYGTGSSRDWAAKGTNLLGVKAVITESFERIHRSNLIGMGILPLQFKEG 819
               LV++AGKEYGTGSSRDWAAKGT LLGV+AVI ES+ERIHRSNLIGMG++PLQF EG
Sbjct: 783 EGTPLVVVAGKEYGTGSSRDWAAKGTRLLGVRAVIAESYERIHRSNLIGMGVVPLQFPEG 842

Query: 820 TTRKTLKLDGSERISIEISDKLTPGAMVPVTIERQDGDIEKIETLCRIDTADELEYYKNG 879
            +R +L L G E ISI   + L+PG  V V I++ D +   ++  CRIDTA+EL YY++G
Sbjct: 843 ESRTSLGLTGDEEISIAGLNDLSPGGTVKVVIKQGDQE-RTVDAKCRIDTANELAYYRHG 901

Query: 880 GILQYVLRKI 889
           GIL YVLRK+
Sbjct: 902 GILHYVLRKM 911


Lambda     K      H
   0.316    0.134    0.393 

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: 2143
Number of extensions: 97
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: 891
Length of database: 915
Length adjustment: 43
Effective length of query: 848
Effective length of database: 872
Effective search space:   739456
Effective search space used:   739456
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