GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Geobacter metallireducens GS-15

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_004513187.1 GMET_RS05080 aconitate hydratase AcnA

Query= SwissProt::Q5SMF6
         (902 letters)



>NCBI__GCF_000012925.1:WP_004513187.1
          Length = 937

 Score = 1080 bits (2792), Expect = 0.0
 Identities = 553/930 (59%), Positives = 680/930 (73%), Gaps = 39/930 (4%)

Query: 3   NSFQTLKTLTTKSGTYGYYDLQELERKGVAEVSRLPFSIRVMLESLLRNEDGYQVTREDI 62
           +SF++   L      Y Y+ L +      A++SRLP+SI+++LE+LLR EDG  V R+DI
Sbjct: 7   DSFESRAILAVGQSRYHYHSLPKFAESFRADISRLPYSIKILLENLLRREDGVTVERDDI 66

Query: 63  EALARWRPDP-GEINVPLKLARVILQDFTGVPAVVDLAAMRDAIKAKGGDPKRINPVVPA 121
            AL  W P    +  +    ARV+LQDFTGVPA+ DLAAMR A+K  GGDP RINP+ PA
Sbjct: 67  VALGHWHPRTLPDREIQFMPARVLLQDFTGVPAIADLAAMRAALKRLGGDPARINPLQPA 126

Query: 122 DLVIDHSVQVDAFGTAYAFFYNVEKEYERNRERYLLLKWAQNALENFRVVPPGTGIVHQV 181
           DL+IDHSVQVD +GT  A   N + E+ RNRERY  L+W Q A  NFRV+PP TGI HQV
Sbjct: 127 DLIIDHSVQVDRYGTKSAASANADFEFRRNRERYQFLRWGQGAFRNFRVIPPDTGICHQV 186

Query: 182 NIEYLTKVVMTGKRDGLTLAFPDSLVGTDSHTTMVNGLGVLGWGVGGIEAEAVMLGQPYY 241
           N+EYL ++ M  ++DG    +PD+LVGTDSHTTMVNGLGV+GWGVGGIEAEA +LGQP  
Sbjct: 187 NLEYLARIAMVAEQDGENWVYPDTLVGTDSHTTMVNGLGVVGWGVGGIEAEAALLGQPCS 246

Query: 242 MLAPRVVGFKLYGELPEGATATDLVLTVTEMLRKHGVVGKFVEFYGPGVAKLSTPDRATI 301
           ML PRVVGF+  G LP GATATDLVLTVT+MLRK GVVG FVEF+GPG+A L+  DRATI
Sbjct: 247 MLIPRVVGFRFLGRLPPGATATDLVLTVTQMLRKKGVVGAFVEFFGPGLASLTVADRATI 306

Query: 302 ANMAPEYGATMGFFPVDEETLNYLRQTGRPEELVELVEAYTKAVGLFRTPEAEEKVQYSE 361
            NMAPEYGAT+G FPVD +TL+YLR TGR   LV LVEAY +A G++   +  E   YS+
Sbjct: 307 GNMAPEYGATIGIFPVDGQTLDYLRLTGR-AALVPLVEAYYRAQGMWYDADQPEP-WYSD 364

Query: 362 YLELDLSAVEPSLAGPKRPQDRVPLKEVKKSF-----------LAHLTKPVKERGFG--- 407
            +ELDL  VEP LAGP RPQDR+PLKEV+ SF            A + + + +R FG   
Sbjct: 365 TIELDLGTVEPCLAGPSRPQDRIPLKEVRGSFRKSLAGLMQNETARIDRGILDRWFGDGG 424

Query: 408 --------LSED-------QLQRKVLVKRRD-EEFELTHGSVVIAAITSCTNTSNPSVML 451
                   LS          L+R V V++ D   + L HGS+VIAAITSCTNTSNPSV++
Sbjct: 425 APRYVAPELSISPPDEKLGPLERCVPVRQPDGVAYNLCHGSIVIAAITSCTNTSNPSVLM 484

Query: 452 GAGLLAKKAVEAGLDRKPWVKTSLAPGSKVVTDYLEMSGLMPFLEALGFHLVGYGCTTCI 511
            AGLLA+ AV+ GL  KPWVKTS APGS+VVTDYL  +GL  +LE L FHLVGYGCTTCI
Sbjct: 485 AAGLLARNAVQRGLQVKPWVKTSFAPGSRVVTDYLASAGLTAYLEGLRFHLVGYGCTTCI 544

Query: 512 GNSGPLPEDIAKAVEEGNLVVAAVLSGNRNFEGRINPHVKANYLASPMLVVAYALAGRMD 571
           GNSGPLP+ IA+AV +G L VAAVLSGNRNFEGRIN +V+ NYLASP LVVAYALAG + 
Sbjct: 545 GNSGPLPDHIARAVVDGGLAVAAVLSGNRNFEGRINNYVRTNYLASPPLVVAYALAGNIA 604

Query: 572 IDFTTEPLGFDPNGKPIYLKDIWPSMEEIREAIRKTLDPELFKKEYSKVFEGDERWQALP 631
           +D T +P+G DPNG+P+YLKDIWP+ EE+ + +R+ + PE F + Y+ +  G+  W+ LP
Sbjct: 605 MDLTRDPVGIDPNGQPVYLKDIWPADEEVADLVRRHVTPEHFSRGYADILRGNTAWEGLP 664

Query: 632 APTGELYQWDPESTYIQNPPFFEDLG--ERKVEDIRGARVLLVLGDSVTTDHISPAGAIP 689
            P  ELYQW+  STY++ PPFF D+      V+DIRGARVL +LGDSVTTDHISPAGAI 
Sbjct: 665 VPASELYQWEETSTYLKEPPFFADVTAVPAPVDDIRGARVLALLGDSVTTDHISPAGAIA 724

Query: 690 VKSPAGQYLISKGVKPEDFNSYGSRRGNHEVMMRGTFANIRIKNLMLDGIEGGYAKKLP- 748
            +SPAG+YL+S GVKPEDFNSYGSRRGNHEVM+RGTFAN+RI+NL++ G+EGG     P 
Sbjct: 725 PESPAGRYLVSLGVKPEDFNSYGSRRGNHEVMVRGTFANVRIRNLLVPGVEGGMTNYFPQ 784

Query: 749 ---EGDVDFVYNVAMRYKAEGTPLLVIAGKEYGTGSSRDWAAKGTYLLGIRAVLAESFER 805
              +G+   +Y+ AMRY+ +G PL+V+AG EYGTGSSRDWAAKGT LLG+RAV+A+SFER
Sbjct: 785 GKDQGETMPIYDAAMRYQQDGIPLIVVAGAEYGTGSSRDWAAKGTRLLGVRAVIAQSFER 844

Query: 806 IHRSNLVGMGVLPLEFLPGENRETLGLTGYEVYDILGLEDLKPRKLVDIVARREDGSEVR 865
           IHRSNL+GMGVLPL+F+ GE+RET GLTG E Y+I GL  L P   + + AR   G+   
Sbjct: 845 IHRSNLIGMGVLPLQFMAGESRETHGLTGEETYEIEGLASLIPGGTLRVTARSAGGNGRE 904

Query: 866 FQAIARLDTPVEVDYYKNGGILQTVLLNML 895
           FQ + R+DTP E+DYY++GGIL  VL   L
Sbjct: 905 FQVLVRIDTPNELDYYRHGGILPYVLRQTL 934


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: 2403
Number of extensions: 128
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: 902
Length of database: 937
Length adjustment: 43
Effective length of query: 859
Effective length of database: 894
Effective search space:   767946
Effective search space used:   767946
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: 57 (26.6 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