GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Desulfacinum infernum DSM 9756

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_073036524.1 BUB04_RS02125 aconitate hydratase AcnA

Query= SwissProt::Q5SMF6
         (902 letters)



>NCBI__GCF_900129305.1:WP_073036524.1
          Length = 881

 Score =  994 bits (2571), Expect = 0.0
 Identities = 514/881 (58%), Positives = 641/881 (72%), Gaps = 22/881 (2%)

Query: 17  TYGYYDLQELERKGVAEVSRLPFSIRVMLESLLRNEDGYQVTREDIEALARWRPDPGE-I 75
           T+ + DL+ L       + RLP+SIRV+LE+++R  D   VT  D+E LA WR    E +
Sbjct: 13  TFEFVDLKGLFGN---RLGRLPYSIRVLLENVVRRRDDRLVTERDVENLAGWRGRYAEPV 69

Query: 76  NVPLKLARVILQDFTGVPAVVDLAAMRDAIKAKGGDPKRINPVVPADLVIDHSVQVDAFG 135
            +P   ARV++QDFTGVPAV DLAAMRDA+ A G DP  +NP+VP DLV+DHSVQVD FG
Sbjct: 70  EIPFFPARVLMQDFTGVPAVADLAAMRDALVALGKDPAAVNPLVPVDLVVDHSVQVDFFG 129

Query: 136 TAYAFFYNVEKEYERNRERYLLLKWAQNALENFRVVPPGTGIVHQVNIEYLTKVVMTGKR 195
           T+ A   NV +EYERN ERY  LKWAQ + ENFRVVPP +GI HQVN+E+L++V    K 
Sbjct: 130 TSDALTANVRREYERNGERYTFLKWAQKSFENFRVVPPNSGICHQVNLEHLSRVFWDRKE 189

Query: 196 DGLTLAFPDSLVGTDSHTTMVNGLGVLGWGVGGIEAEAVMLGQPYYMLAPRVVGFKLYGE 255
           DG+ + FPD++VG DSHTTMVNG+GVLGWGVGGIEAEAV++GQPY M  P V+G +L G 
Sbjct: 190 DGVRICFPDTVVGLDSHTTMVNGIGVLGWGVGGIEAEAVLMGQPYSMAIPEVIGVRLVGR 249

Query: 256 LPEGATATDLVLTVTEMLRKHGVVGKFVEFYGPGVAKLSTPDRATIANMAPEYGATMGFF 315
           LP  A ATDLVL VTE LR +GVV KFVEF+GP V  LS P RATIANM+PEYGAT+GFF
Sbjct: 250 LPRRANATDLVLRVTEALRDYGVVEKFVEFFGPAVTALSVPARATIANMSPEYGATVGFF 309

Query: 316 PVDEETLNYLRQTGRPEELVELVEAYTKAVGLFRTPEAEEKVQYSEYLELDLSAVEPSLA 375
           PVDE+ + YLR T R E    + EA  +A+GL+   +  E+  Y++ LE+DLSA+ P++A
Sbjct: 310 PVDEKVVEYLRLTHR-ERQARVTEAAARAMGLYY--DGSEEPDYTDVLEIDLSAIRPAVA 366

Query: 376 GPKRPQDRVPLKEVKKSFLAHLTKPVKERGFGLSEDQLQRKVLVKRRDEEFELTHGSVVI 435
           GP +P+DR+ L E+K  F        + RG    ED  +  V V+ R E  EL+ GSVVI
Sbjct: 367 GPSKPKDRIELSELKTRFR-------QLRG----EDAPKAAVPVRIRGENVELSDGSVVI 415

Query: 436 AAITSCTNTSNPSVMLGAGLLAKKAVEAGLDRKPWVKTSLAPGSKVVTDYLEMSGLMPFL 495
           AAITSCTNTSNP  +LGA LLA+ AV+ GL     VKTSLAPGSKVV  YL+ SGL+P+L
Sbjct: 416 AAITSCTNTSNPHALLGAALLARNAVKRGLAVPAHVKTSLAPGSKVVVQYLDRSGLLPYL 475

Query: 496 EALGFHLVGYGCTTCIGNSGPLPEDIAKAVEEGNLVVAAVLSGNRNFEGRINPHVKANYL 555
           EALGFH V +GCTTCIGNSGPL  ++ +A+EE NL VAAVLSGNRNFE RI+  VK+N+L
Sbjct: 476 EALGFHPVAFGCTTCIGNSGPLHPEVERAIEEHNLNVAAVLSGNRNFEARIHQKVKSNFL 535

Query: 556 ASPMLVVAYALAGRMDIDFTTEPLGFDPNGKPIYLKDIWPSMEEIREAIRKTLDPELFKK 615
           ASP+LVVA+ALAGR+D+D   EP+G DPNG P++L DI P  EEI E + + +  +LF++
Sbjct: 536 ASPLLVVAFALAGRVDVDLEKEPVGLDPNGGPVFLADILPDDEEIEELVNRYVQEDLFRE 595

Query: 616 EYSKVFEGDERWQALPAPTGELYQWDPESTYIQNPPFFEDLGERKVE--DIRGARVLLVL 673
            Y K+ EGD+ W  L       Y WDP STYI+ PP+FE    +  E  DIRGARVLL L
Sbjct: 596 TYEKILEGDQFWNELQVQESVTYPWDPRSTYIKCPPYFEGFTPQMPETTDIRGARVLLWL 655

Query: 674 GDSVTTDHISPAGAIPVKSPAGQYLISKGVKPEDFNSYGSRRGNHEVMMRGTFANIRIKN 733
           GD+VTTDHISPAGAI    PAG+YL S G+  ++FNSYG+RRGNHEVMMRGTFANIRI+N
Sbjct: 656 GDAVTTDHISPAGAIHEDYPAGRYLKSLGLSRQEFNSYGARRGNHEVMMRGTFANIRIRN 715

Query: 734 LMLDGIEGGYAKKLPEGDVDFVYNVAMRYKAEGTPLLVIAGKEYGTGSSRDWAAKGTYLL 793
            ++    G +  K PEG+  +V+  A  Y+ EG PL+V+ GKEYGTGSSRDWAAKG  LL
Sbjct: 716 KLVSE-PGSFTVKFPEGERMYVFEAAEAYRREGVPLIVLGGKEYGTGSSRDWAAKGPKLL 774

Query: 794 GIRAVLAESFERIHRSNLVGMGVLPLEFLPGENRETLGLTGYEVYDILGLEDLKPRKLVD 853
           G++AV+AESFERIHRSNL+GMG+LPL+FL GE+ E+LGL G E Y I G+  ++PR+ + 
Sbjct: 775 GVKAVIAESFERIHRSNLIGMGILPLQFLEGESAESLGLDGTEEYHIAGIAGIEPRRKLT 834

Query: 854 IVARREDGSEVRFQAIARLDTPVEVDYYKNGGILQTVLLNM 894
           + A + DG E  FQ +ARLDT +E DYY+NGGIL  VL  M
Sbjct: 835 VTAVK-DGKEKTFQVLARLDTEIEADYYRNGGILDYVLRKM 874


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: 2161
Number of extensions: 87
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: 902
Length of database: 881
Length adjustment: 43
Effective length of query: 859
Effective length of database: 838
Effective search space:   719842
Effective search space used:   719842
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: 56 (26.2 bits)

This GapMind analysis is from Apr 09 2024. 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