GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Nitratifractor salsuginis DSM 16511

Align Aconitate hydratase B; 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_013553742.1 NITSA_RS04000 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= SwissProt::Q8ZRS8
         (865 letters)



>NCBI__GCF_000186245.1:WP_013553742.1
          Length = 857

 Score = 1097 bits (2836), Expect = 0.0
 Identities = 553/860 (64%), Positives = 674/860 (78%), Gaps = 22/860 (2%)

Query: 1   MLEEYRKHVAERAAQGIVPKPLDATQMAALVELLKTPPVGEEEFLLDLLINRVPPGVDEA 60
           ++E+Y+KH  ERA  G+ P PL A Q A LVELLK  P+ EEE+LLDLL N V PGVD+A
Sbjct: 3   LIEDYKKHTEERAKLGVPPLPLTAQQTAELVELLKQDPIPEEEYLLDLLKNHVNPGVDDA 62

Query: 61  AYVKAGFLAAVAKGDTTSPLVSPEKAIELLGTMQGGYNIHPLIDAL--DDAKLAPIAAKA 118
           AYVKA FL  + +G   S  +SP +A+ +LG M GGYN+ PL+DAL   DA++A  AA  
Sbjct: 63  AYVKAAFLNDIVQGKAQSKAISPVEAVRILGMMLGGYNVGPLVDALKHSDAEIAQAAADE 122

Query: 119 LSHTLLMFDNFYDVEEKAKAGNEYAKQVMQSWADAEWFLSRPPLAEKITVTVFKVTGETN 178
           L HT+L++D F DV+E    GNEYAKQV++SWA+AEWFL+R PL E++ +TVFKV GETN
Sbjct: 123 LKHTILVYDAFNDVKELMDQGNEYAKQVIESWANAEWFLNREPLPEEMKLTVFKVPGETN 182

Query: 179 TDDLSPAPDAWSRPDIPLHAQAMLKNAREGIEPDQPGVVGPIKQIEALQKKGYPLAYVGD 238
           TDDLSPA +A++R DIPLHAQ+ML N  +           P++ I+ L+++G  LAYVGD
Sbjct: 183 TDDLSPASEAFTRSDIPLHAQSMLVNRMDN----------PLETIKKLKERGNDLAYVGD 232

Query: 239 VVGTGSSRKSATNSVLWFMGDDIPNVPNKRGGGLCLGGKIAPIFFNTMEDAGALPIEVDV 298
           VVGTGSSRKS  NSV W+ G DIP VPNKR GG+ +G  IAPIFFNT ED+G LPIE  V
Sbjct: 233 VVGTGSSRKSGINSVQWWFGHDIPGVPNKRTGGVVIGSIIAPIFFNTAEDSGCLPIEAPV 292

Query: 299 SNLNMGDVIDVYPYKGEVRNHETGELLATFELKTDVLIDEVRAGGRIPLIIGRGLTTKAR 358
             L  GD I V PY+G++  +  GE+++ F LK + L DE+RAGGRIPLIIG+GLT KAR
Sbjct: 293 DALETGDEIVVKPYEGKILKN--GEVVSEFTLKPNTLPDEMRAGGRIPLIIGKGLTNKAR 350

Query: 359 EALGLPHSDVFRQAKDVAESSRGFSLAQKMVGRACGVKGIRPGAYCEPKMTSVGSQDTTG 418
           EALGL HSDVF + +  A+S +G++LAQKMVG+ACG++G+RPG Y EP +T+VGSQDTTG
Sbjct: 351 EALGLGHSDVFTKPEQPADSGKGYTLAQKMVGKACGMEGVRPGMYVEPVVTTVGSQDTTG 410

Query: 419 PMTRDELKDLACLGFSADLVMQSFCHTAAYPKPVDVTTHHTLPDFIMNRGGVSLRPGDGV 478
           PMTRDE+K+LA L F ADLV+Q+FCHTAAYPKP DV   HTLP F  +RGGV L+PGDGV
Sbjct: 411 PMTRDEIKELAALSFGADLVLQTFCHTAAYPKPADVELQHTLPPFWTSRGGVILKPGDGV 470

Query: 479 IHSWLNRMLLPDTVGTGGDSHTRFPIGISFPAGSGLVAFAAATGVMPLDMPESVLVRFKG 538
           IHSWLNRM+LPDTVGTGGDSHTRFPIGISFPAGSGLVAFAA TG+MPL+MPESVLV+FKG
Sbjct: 471 IHSWLNRMILPDTVGTGGDSHTRFPIGISFPAGSGLVAFAAVTGMMPLNMPESVLVKFKG 530

Query: 539 KMQPGITLRDLVHAIPLYAIKQGLLTVEKKGKKNIFSGRILEIEGLPDLKVEQAFELTDA 598
           +MQPGITLRDLV+AIP  AIK+GLLTVEKKGKKN+F+GRILEIEGL DLKVEQAFEL+DA
Sbjct: 531 EMQPGITLRDLVNAIPYQAIKEGLLTVEKKGKKNVFAGRILEIEGLEDLKVEQAFELSDA 590

Query: 599 SAERSAAGCTIKLNKEPIVEYLTSNIVLLKWMIAEGYGDRRTLERRIQGMEKWLADPQLL 658
           SAERSAA CT+KLNKEP++EYL SNI LL+ MI +GY D+RTL+RRI  M+ WL +P L+
Sbjct: 591 SAERSAAACTVKLNKEPVIEYLRSNIKLLEKMIEQGYEDKRTLQRRIDKMKAWLENPTLM 650

Query: 659 EADADAEYAAVIDIDLADIKEPILCAPNDPDDARLLSDVQGEK-----IDEVFIGSCMTN 713
           E D DAEYAAVI+IDL +I EPI+  PNDPDD   LS+V  ++     IDEVF+GSCMTN
Sbjct: 651 ERDEDAEYAAVIEIDLNEITEPIVACPNDPDDVATLSEVLADEKRPKNIDEVFVGSCMTN 710

Query: 714 IGHFRAAGKLLDNHKGQLPTRLWVAPPTRMDAAQLTEEGYYSVFGKSGARIEIPGCSLCM 773
           IG FRA G++L   +G + TRLWV PPT+MD  +L EEGYY++FG++GAR EIPGCSLCM
Sbjct: 711 IGLFRALGEVLKG-EGPVDTRLWVTPPTKMDQKELIEEGYYAIFGQAGARTEIPGCSLCM 769

Query: 774 GNQARVADGATVVSTSTRNFPNRLGTGANVFLASAELAAVAALIGKLPTPEEYQTYVAQ- 832
           GNQARV D + V STSTRNF NR+G GA V+L S+ELAAV AL+G++P+ EEY   V + 
Sbjct: 770 GNQARVRDNSVVFSTSTRNFDNRMGKGAQVYLGSSELAAVCALLGRIPSKEEYLEIVNKK 829

Query: 833 -VDKTAVDTYRYLNFDQLSQ 851
             D      Y+YLNFDQ+ +
Sbjct: 830 ITDDKKDQVYKYLNFDQIPE 849


Lambda     K      H
   0.317    0.136    0.400 

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: 2001
Number of extensions: 81
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: 865
Length of database: 857
Length adjustment: 42
Effective length of query: 823
Effective length of database: 815
Effective search space:   670745
Effective search space used:   670745
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 (21.7 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