GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Caminibacter mediatlanticus TB-2

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_007474665.1 CMTB2_RS05535 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= SwissProt::Q8ZRS8
         (865 letters)



>NCBI__GCF_000170735.1:WP_007474665.1
          Length = 861

 Score = 1083 bits (2800), Expect = 0.0
 Identities = 547/859 (63%), Positives = 677/859 (78%), Gaps = 24/859 (2%)

Query: 2   LEEYRKHVAERAAQGIVPKPLDATQMAALVELLKTPPVGEEEFLLDLLINRVPPGVDEAA 61
           +EEY+KH  ERA  GI P PL A Q A LVELLK  P+ EEE+L+DL +N + PGVDEAA
Sbjct: 4   IEEYKKHTEERAKLGIPPLPLTAAQTAELVELLKKVPIVEEEYLMDLFLNHINPGVDEAA 63

Query: 62  YVKAGFLAAVAKGDTTSPLVSPEKAIELLGTMQGGYNIHPLIDAL--DDAKLAPIAAKAL 119
           YVKA FL  + +G  +SP +S ++A+E+LGTM GGYN+ PLIDAL  +D ++A  AA  L
Sbjct: 64  YVKAAFLNDIVQGKASSPAISKKRAVEILGTMLGGYNVKPLIDALSHEDEEVAKEAANQL 123

Query: 120 SHTLLMFDNFYDVEEKAKAGNEYAKQVMQSWADAEWFLSRPPLAEKITVTVFKVTGETNT 179
            +TLL++D F+DV+E A  GN+YAK+V++SW++AEWF S+ PL EKI   VFKV GETNT
Sbjct: 124 KNTLLVYDAFHDVKELADKGNKYAKEVLESWSEAEWFTSKKPLPEKIEAIVFKVPGETNT 183

Query: 180 DDLSPAPDAWSRPDIPLHAQAMLKNAREGIEPDQPGVVGPIKQIEALQKKGYPLAYVGDV 239
           DDLSPA +A++R DIPLHA +MLK       PD       I++I  L+K G P+A+VGDV
Sbjct: 184 DDLSPASEAFTRSDIPLHALSMLKAKM----PDA------IEKINELKKSGKPVAFVGDV 233

Query: 240 VGTGSSRKSATNSVLWFMGDDIPNVPNKRGGGLCLGGKIAPIFFNTMEDAGALPIEVDVS 299
           VGTGSSRKSA NSV+W +G++IP VPNK+ GG+ +GG IAPIFFNT+ED+GALPI+  V 
Sbjct: 234 VGTGSSRKSAANSVIWHIGEEIPYVPNKKRGGIVIGGVIAPIFFNTLEDSGALPIQAPVD 293

Query: 300 NLNMGDVIDVYPYKGEVRNHETGELLATFELKTDVLIDEVRAGGRIPLIIGRGLTTKARE 359
            L  GD+I++YPY+G++  +  GE+++ FEL  + L DEVRAGGR+PLIIG+ LT KARE
Sbjct: 294 KLETGDIIEIYPYEGKIVKN--GEVVSEFELSPNTLPDEVRAGGRVPLIIGKNLTKKARE 351

Query: 360 ALGLPHSDVF-RQAKDVAESSRGFSLAQKMVGRACGVKGIRPGAYCEPKMTSVGSQDTTG 418
            LG    ++F R A+   +   G++ AQK++G+ACG++G+RPG Y EP  T+VGSQDTTG
Sbjct: 352 VLGKEEENIFIRPAQPEDKKGVGYTQAQKIIGKACGMEGVRPGMYVEPTATTVGSQDTTG 411

Query: 419 PMTRDELKDLACLGFSADLVMQSFCHTAAYPKPVDVTTHHTLPDFIMNRGGVSLRPGDGV 478
            MTRDE+K+LA LGF+ADLVMQSFCHTAAYPKP D+  HHTLPDFI +RGGV+LRPGDGV
Sbjct: 412 AMTRDEIKELAALGFNADLVMQSFCHTAAYPKPADIKLHHTLPDFITSRGGVALRPGDGV 471

Query: 479 IHSWLNRMLLPDTVGTGGDSHTRFPIGISFPAGSGLVAFAAATGVMPLDMPESVLVRFKG 538
           IHSWLNRM+LPDT+GTGGDSHTRFPIGISFPAGSGLVAFAA TG MPL++PESVLVRFKG
Sbjct: 472 IHSWLNRMILPDTLGTGGDSHTRFPIGISFPAGSGLVAFAAVTGSMPLNVPESVLVRFKG 531

Query: 539 KMQPGITLRDLVHAIPLYAIKQGLLTVEKKGKKNIFSGRILEIEG--LPDLKVEQAFELT 596
           ++QPGITLRDLV+AIP +AIKQGLLTVEKK KKNIF+GRILEIEG  +  L VEQAFEL 
Sbjct: 532 ELQPGITLRDLVNAIPYFAIKQGLLTVEKKNKKNIFNGRILEIEGDIIRTLTVEQAFELA 591

Query: 597 DASAERSAAGCTIKLNKEPIVEYLTSNIVLLKWMIAEGYGDRRTLERRIQGMEKWLADPQ 656
           DASAERSAA CT+ +++E + EYL SNI LL+ MI  GY D+RTL+RRI  M++WL +P+
Sbjct: 592 DASAERSAAACTVDVSEEQVAEYLKSNIKLLEEMIEAGYEDKRTLQRRIDKMKEWLDNPK 651

Query: 657 LLEADADAEYAAVIDIDLADIKEPILCAPNDPDDARLLSDVQGE-----KIDEVFIGSCM 711
           LL  D DAEYAAVI+IDL +I EPI+  PNDPDD   +S+V  +     KIDEVF+GSCM
Sbjct: 652 LLRRDEDAEYAAVIEIDLNEITEPIVACPNDPDDVATISEVLADPNRPHKIDEVFLGSCM 711

Query: 712 TNIGHFRAAGKLLDNHKGQLPTRLWVAPPTRMDAAQLTEEGYYSVFGKSGARIEIPGCSL 771
           TNIGH+RAAG++L   +GQ+P RLW+APPT+MD AQL EEGYYS+FG++GARIEIPGCSL
Sbjct: 712 TNIGHYRAAGEILKG-EGQVPVRLWIAPPTKMDKAQLIEEGYYSIFGQAGARIEIPGCSL 770

Query: 772 CMGNQARVADGATVVSTSTRNFPNRLGTGANVFLASAELAAVAALIGKLPTPEEYQTYVA 831
           CMGNQARVAD A V STSTRNF NR+G GA V+L SAELAAV AL+G++PT EEY   + 
Sbjct: 771 CMGNQARVADYANVFSTSTRNFDNRMGKGAKVYLGSAELAAVIALLGRIPTKEEYLEIIE 830

Query: 832 QVDKTAVD-TYRYLNFDQL 849
           +      D  Y YLNF ++
Sbjct: 831 KKLAGKEDKVYNYLNFHKM 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: 1986
Number of extensions: 84
Number of successful extensions: 8
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: 861
Length adjustment: 42
Effective length of query: 823
Effective length of database: 819
Effective search space:   674037
Effective search space used:   674037
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.

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