GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Acidovorax sp. GW101-3H11

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 Ac3H11_3150 Aconitate hydratase 2 (EC 4.2.1.3) @ 2-methylisocitrate dehydratase (EC 4.2.1.99)

Query= SwissProt::Q8ZRS8
         (865 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3150
          Length = 866

 Score = 1242 bits (3214), Expect = 0.0
 Identities = 628/863 (72%), Positives = 711/863 (82%), Gaps = 8/863 (0%)

Query: 1   MLEEYRKHVAERAAQGIVPKPLDATQMAALVELLKTPPVGEEEFLLDLLINRVPPGVDEA 60
           ML+ YR HVAERAA GI P PLDA Q+A L+EL+K PP GE+ FLLDLL +RVPPGVD+A
Sbjct: 1   MLKAYRDHVAERAALGIPPLPLDAKQVAELIELIKNPPAGEDAFLLDLLTHRVPPGVDDA 60

Query: 61  AYVKAGFLAAVAKGDTTSPLVSPEKAIELLGTMQGGYNIHPLIDALDDAKLAPIAAKALS 120
           A VKA FLAAVA GD    L+S  KA ELLGTM GGYN+HPLI+ LDDA++A +AA AL 
Sbjct: 61  AKVKASFLAAVAHGDVKVGLISKSKATELLGTMVGGYNVHPLIELLDDAEVAGVAADALK 120

Query: 121 HTLLMFDNFYDVEEKAKAGNEYAKQVMQSWADAEWFLSRPPLAEKITVTVFKVTGETNTD 180
            TLLMFD F DV  KAKAGN  A++VMQSWA+AEWF SRP + +KITVTVFKV GETNTD
Sbjct: 121 KTLLMFDFFNDVATKAKAGNAKAQEVMQSWANAEWFTSRPEVEKKITVTVFKVPGETNTD 180

Query: 181 DLSPAPDAWSRPDIPLHAQAMLKNARE--GIEPDQPGVVGPIKQIEALQKKGYPLAYVGD 238
           DLSPAPDAWSRPDIPLH  AMLKN R     +P++ G  GP++ I+ L+KKG+ +AYVGD
Sbjct: 181 DLSPAPDAWSRPDIPLHYLAMLKNTRPDAAFKPEEDGKRGPMQFIDDLKKKGHLVAYVGD 240

Query: 239 VVGTGSSRKSATNSVLWFMGDDIPNVPNKRGGGLCLGGKIAPIFFNTMEDAGALPIEVDV 298
           VVGTGSSRKSATNS++W  G DIP VPNKR GG+ LGGKIAPIFFNT ED+G+LPIEVDV
Sbjct: 241 VVGTGSSRKSATNSIVWATGQDIPFVPNKRFGGVTLGGKIAPIFFNTQEDSGSLPIEVDV 300

Query: 299 SNLNMGDVIDVYPYKGEVRNHETGELLATFELKTDVLIDEVRAGGRIPLIIGRGLTTKAR 358
           S L MGDVIDV PY G++   + G  +A F+LK+DVL DEVRAGGRI LIIGR LT KAR
Sbjct: 301 SKLEMGDVIDVLPYDGKIV--KDGATVAEFQLKSDVLFDEVRAGGRINLIIGRSLTAKAR 358

Query: 359 EALGLPHSDVFRQAKDVAESSRGFSLAQKMVGRACGV---KGIRPGAYCEPKMTSVGSQD 415
           E LGLP S  FR       ++ GF+LAQKMVGRA G+   +G+RPG YCEPKMT+VGSQD
Sbjct: 359 EFLGLPASTAFRLPTAPVATNAGFTLAQKMVGRAVGLPEGQGVRPGTYCEPKMTTVGSQD 418

Query: 416 TTGPMTRDELKDLACLGFSADLVMQSFCHTAAYPKPVDVTTHHTLPDFIMNRGGVSLRPG 475
           TTGPMTRDELKDLACLGFSADLVMQSFCHTAAYPKPVDV TH  LP FI NRGGV+LRPG
Sbjct: 419 TTGPMTRDELKDLACLGFSADLVMQSFCHTAAYPKPVDVKTHRELPAFISNRGGVALRPG 478

Query: 476 DGVIHSWLNRMLLPDTVGTGGDSHTRFPIGISFPAGSGLVAFAAATGVMPLDMPESVLVR 535
           DGVIHSWLNR+LLPDTVGTGGDSHTRFPIGISFPAGSGLVAF AATGVMPLDMPES+LVR
Sbjct: 479 DGVIHSWLNRLLLPDTVGTGGDSHTRFPIGISFPAGSGLVAFGAATGVMPLDMPESILVR 538

Query: 536 FKGKMQPGITLRDLVHAIPLYAIKQGLLTVEKKGKKNIFSGRILEIEGLPDLKVEQAFEL 595
           FKG MQPG+TLRDLVHAIPLYAIK GLLTV K GK N FSGRILEIEGLPDLKVEQAFEL
Sbjct: 539 FKGDMQPGVTLRDLVHAIPLYAIKAGLLTVAKAGKINAFSGRILEIEGLPDLKVEQAFEL 598

Query: 596 TDASAERSAAGCTIKLNKEPIVEYLTSNIVLLKWMIAEGYGDRRTLERRIQGMEKWLADP 655
           +DASAERSAAGCTIKLN EPI EYLTSNIVL+K MIA+GY D +TL+RRI+ +E WLA P
Sbjct: 599 SDASAERSAAGCTIKLNPEPIKEYLTSNIVLMKNMIADGYADAKTLQRRIEKVEAWLAKP 658

Query: 656 QLLEADADAEYAAVIDIDLADIKEPILCAPNDPDDARLLSDVQGEKIDEVFIGSCMTNIG 715
            LLEAD DAEYAAVI+IDLADIKEPI+C PNDPDDA+ LS+V G KIDE FIGSCMTNIG
Sbjct: 659 DLLEADKDAEYAAVIEIDLADIKEPIVCCPNDPDDAKFLSEVSGTKIDEAFIGSCMTNIG 718

Query: 716 HFRAAGKLLDNHKGQLPTRLWVAPPTRMDAAQLTEEGYYSVFGKSGARIEIPGCSLCMGN 775
           HFRAA KLL   +  +P +LWVAPPT+MD ++L +EG+Y+ FG +GAR E+PGCSLCMGN
Sbjct: 719 HFRAAAKLLGGQR-DIPVKLWVAPPTKMDESELIKEGHYAAFGTAGARTEMPGCSLCMGN 777

Query: 776 QARVADGATVVSTSTRNFPNRLGTGANVFLASAELAAVAALIGKLPTPEEYQTYVAQVDK 835
           QA+V +GATV+STSTRNFPNRLG   NVFL SAELAA+A+ +G LP+ EEY   +  +D 
Sbjct: 778 QAQVREGATVISTSTRNFPNRLGKNTNVFLGSAELAAIASRLGYLPSKEEYLKEMGVIDA 837

Query: 836 TAVDTYRYLNFDQLSQYTEKADG 858
                YRY+NFDQ+ +Y E A G
Sbjct: 838 DKASVYRYMNFDQIEEYAEAAKG 860


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: 2070
Number of extensions: 76
Number of successful extensions: 5
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: 866
Length adjustment: 42
Effective length of query: 823
Effective length of database: 824
Effective search space:   678152
Effective search space used:   678152
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 17 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