GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Derxia gummosa DSM 723

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_028313028.1 H566_RS0121290 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= SwissProt::Q8ZRS8
         (865 letters)



>NCBI__GCF_000482785.1:WP_028313028.1
          Length = 863

 Score = 1273 bits (3294), Expect = 0.0
 Identities = 647/864 (74%), Positives = 728/864 (84%), Gaps = 8/864 (0%)

Query: 1   MLEEYRKHVAERAAQGIVPKPLDATQMAALVELLKTPPVGEEEFLLDLLINRVPPGVDEA 60
           MLE YR+HVAERAA GI P PL A Q A L+EL+K PP GEE+FL++LL  RVPPGVD+A
Sbjct: 1   MLETYRQHVAERAALGIPPLPLSAQQTADLIELIKNPPAGEEDFLVELLTFRVPPGVDDA 60

Query: 61  AYVKAGFLAAVAKGDTTSPLVSPEKAIELLGTMQGGYNIHPLIDALDDAKLAPIAAKALS 120
           A VKA FLAAVA GD    L+S  KA ELLGTM GGYN+ PLID L+D ++A IAA+ L 
Sbjct: 61  AKVKASFLAAVAHGDIKVGLISKAKATELLGTMVGGYNVKPLIDLLEDGEVAAIAAEGLK 120

Query: 121 HTLLMFDNFYDVEEKAKAGNEYAKQVMQSWADAEWFLSRPPLAEKITVTVFKVTGETNTD 180
            TLLMFD F+DV EKAKAGN  AK+V+QSWADAEWF +RP + + ITVTVFKV GETNTD
Sbjct: 121 KTLLMFDFFHDVAEKAKAGNAKAKEVIQSWADAEWFTTRPEVPKSITVTVFKVPGETNTD 180

Query: 181 DLSPAPDAWSRPDIPLHAQAMLKNARE--GIEPDQPGVVGPIKQIEALQKKGYPLAYVGD 238
           DLSPAPDAWSRPDIP+H  AMLKN R     +P++ G  GP++ IE L+KKG+ +AYVGD
Sbjct: 181 DLSPAPDAWSRPDIPMHYLAMLKNTRPDAAFKPEEDGKRGPMQFIEDLKKKGHLVAYVGD 240

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

Query: 299 SNLNMGDVIDVYPYKGEVRNHETGELLATFELKTDVLIDEVRAGGRIPLIIGRGLTTKAR 358
           S L MGDVI+V PY G++   + G  +A F LK++VL+DEVRAGGRI LIIGR LT KAR
Sbjct: 301 SKLEMGDVIEVLPYDGKIT--KDGATVAEFALKSEVLLDEVRAGGRINLIIGRSLTGKAR 358

Query: 359 EALGLPHSDVFRQAKDVAESSRGFSLAQKMVGRACGV---KGIRPGAYCEPKMTSVGSQD 415
           E LGLP S +FR  K   +S +GFSLAQKMVGRA G+   +G+RPG YCEPKMT+VGSQD
Sbjct: 359 EFLGLPASTLFRLPKAPVDSGKGFSLAQKMVGRAVGLPEGQGVRPGTYCEPKMTTVGSQD 418

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

Query: 476 DGVIHSWLNRMLLPDTVGTGGDSHTRFPIGISFPAGSGLVAFAAATGVMPLDMPESVLVR 535
           DGVIHSWLNR+LLPDTVGTGGDSHTRFPIGISFPAGSGLVAF AATGVMPLDMPESVLVR
Sbjct: 479 DGVIHSWLNRLLLPDTVGTGGDSHTRFPIGISFPAGSGLVAFGAATGVMPLDMPESVLVR 538

Query: 536 FKGKMQPGITLRDLVHAIPLYAIKQGLLTVEKKGKKNIFSGRILEIEGLPDLKVEQAFEL 595
           F GKMQPGITLRDLVHAIPLYAIK GLLTVEKKGKKNIFSGRILEIEGLPDLKVEQAFEL
Sbjct: 539 FSGKMQPGITLRDLVHAIPLYAIKAGLLTVEKKGKKNIFSGRILEIEGLPDLKVEQAFEL 598

Query: 596 TDASAERSAAGCTIKLNKEPIVEYLTSNIVLLKWMIAEGYGDRRTLERRIQGMEKWLADP 655
           +DASAERSAAGC IKLNKEPI EYL SNIVL+K MIA+GY D+RTLERRI+ +E WLA+P
Sbjct: 599 SDASAERSAAGCAIKLNKEPIAEYLKSNIVLMKNMIADGYQDKRTLERRIKSVEAWLANP 658

Query: 656 QLLEADADAEYAAVIDIDLADIKEPILCAPNDPDDARLLSDVQGEKIDEVFIGSCMTNIG 715
           QLLEADADAEYAAVI+I+L DIKEPILCAPNDPDDARLLSDV G KIDEVFIGSCMTNIG
Sbjct: 659 QLLEADADAEYAAVIEINLDDIKEPILCAPNDPDDARLLSDVAGTKIDEVFIGSCMTNIG 718

Query: 716 HFRAAGKLLDNHKGQLPTRLWVAPPTRMDAAQLTEEGYYSVFGKSGARIEIPGCSLCMGN 775
           HFRAA KLL   K  +P +LWVAPPT+MDAA+LT+EG+Y+VFG +GAR E+PGCSLCMGN
Sbjct: 719 HFRAASKLLGGQK-DIPVKLWVAPPTKMDAAELTKEGHYNVFGTAGARTEMPGCSLCMGN 777

Query: 776 QARVADGATVVSTSTRNFPNRLGTGANVFLASAELAAVAALIGKLPTPEEYQTYVAQVDK 835
           QA+V  GATVVSTSTRNFPNRLG   NVFLASAELA++A+ +GKLPT  EY  Y+  ++ 
Sbjct: 778 QAQVRTGATVVSTSTRNFPNRLGKDTNVFLASAELASIASKLGKLPTVAEYNEYIGVINA 837

Query: 836 TAVDTYRYLNFDQLSQYTEKADGV 859
            A + YRY+NFDQ+++Y + A  V
Sbjct: 838 DAANIYRYMNFDQIAEYADVAKTV 861


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: 83
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: 863
Length adjustment: 42
Effective length of query: 823
Effective length of database: 821
Effective search space:   675683
Effective search space used:   675683
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