GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Nocardioides dokdonensis FR1436

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_068112647.1 I601_RS17670 aconitate hydratase

Query= SwissProt::O53166
         (943 letters)



>NCBI__GCF_001653335.1:WP_068112647.1
          Length = 936

 Score = 1313 bits (3397), Expect = 0.0
 Identities = 658/946 (69%), Positives = 767/946 (81%), Gaps = 22/946 (2%)

Query: 5   SVNSFGAHDTLKVGEKSYQIYRLDAVP----NTAKLPYSLKVLAENLLRNEDGSNITKDH 60
           S +SFGA  TL V   SY+I+RLDAV     + A LP+SLKVL ENLLR EDGS+IT D 
Sbjct: 3   SKDSFGAKGTLDVDGTSYEIFRLDAVSGDGLDVASLPFSLKVLLENLLRTEDGSDITADD 62

Query: 61  IEAIANWDPKAEPSIEIQYTPARVVMQDFTGVPCIVDLATMREAIADLGGNPDKVNPLAP 120
           ++AIA WD  A+PS EIQ+TPARV+MQDFTGVPC+VDLATMREA+ADLGG+P K+NPLAP
Sbjct: 63  VKAIAGWDADADPSQEIQFTPARVIMQDFTGVPCVVDLATMREAMADLGGDPTKINPLAP 122

Query: 121 ADLVIDHSVIADLFGRADAFERNVEIEYQRNGERYQFLRWGQGAFDDFKVVPPGTGIVHQ 180
           A++VIDHSVIAD+FG  +AF RNVEIEY+RN ERYQFLRWGQGAFDDFKVVPPGTGIVHQ
Sbjct: 123 AEMVIDHSVIADVFGTPEAFGRNVEIEYERNRERYQFLRWGQGAFDDFKVVPPGTGIVHQ 182

Query: 181 VNIEYLASVVMTR--DGV--AYPDTCVGTDSHTTMVNGLGVLGWGVGGIEAEAAMLGQPV 236
           VNIE+LA  V TR  DGV  AYPDTCVGTDSHTTMVNG+GV+GWGVGGIEAEAAMLGQPV
Sbjct: 183 VNIEHLARTVFTREVDGVLQAYPDTCVGTDSHTTMVNGIGVVGWGVGGIEAEAAMLGQPV 242

Query: 237 SMLIPRVVGFRLTGEIQPGVTATDVVLTVTEMLRQHGVVGKFVEFYGEGVAEVPLANRAT 296
           SMLIPRVVGF+L G++  G TATD+VLT+TEMLR+HGVVGKFVEFYG GV+ +PLANRAT
Sbjct: 243 SMLIPRVVGFKLNGDLPEGATATDLVLTITEMLREHGVVGKFVEFYGPGVSVLPLANRAT 302

Query: 297 LGNMSPEFGSTAAIFPIDEETIKYLRFTGRTPEQVALVEAYAKAQGMWHDPKHEPEFSEY 356
           +GNMSPEFGST A+FPIDEET KYL  TGRTPEQ+ALVEAYAK QG+WHDP  EP FSE 
Sbjct: 303 IGNMSPEFGSTIAVFPIDEETTKYLELTGRTPEQIALVEAYAKEQGLWHDPDAEPRFSEK 362

Query: 357 LELNLSDVVPSIAGPKRPQDRIALAQAKSTFREQIYHYVGNGSPDSPHDPHSKLDEVVEE 416
           LEL+L+ VVPS+AGPKRPQDR++L++AK +FR  +  Y    + D+        DE VEE
Sbjct: 363 LELDLATVVPSLAGPKRPQDRVSLSEAKESFRSALADY----AEDTDAQETKGYDENVEE 418

Query: 417 TFPASDPGQLTFANDDVATDETVHSAAAH-ADGRVSNPVRVKSDELGEFVLDHGAVVIAA 475
           +FPASD    T  N         H AA   A GR  NP +V   +   F LDHGAV IAA
Sbjct: 419 SFPASD----TPHNGHGEAPPNGHVAAGSGAGGRPRNPAQVTLADGTSFELDHGAVTIAA 474

Query: 476 ITSCTNTSNPEVMLGAALLARNAVEKGLTSKPWVKTTIAPGSQVVNDYYDRSGLWPYLEK 535
           ITSCTNTSNP VM+GAALLA+ AVEKGL  KPWVKTT+APGS+VV+DYY++SGL PYL+K
Sbjct: 475 ITSCTNTSNPSVMIGAALLAKKAVEKGLERKPWVKTTLAPGSKVVSDYYEKSGLTPYLDK 534

Query: 536 LGFYLVGYGCTTCIGNSGPLPEEISKAVNDNDLSVTAVLSGNRNFEGRINPDVKMNYLAS 595
           LGF LVGYGCTTCIGNSGPL  E+S+AVNDNDL+V +VLSGNRNFEGRINPDVKMNYLAS
Sbjct: 535 LGFNLVGYGCTTCIGNSGPLIPEVSQAVNDNDLAVVSVLSGNRNFEGRINPDVKMNYLAS 594

Query: 596 PPLVIAYALAGTMDFDFQTQPLGQDKDGKNVFLRDIWPSQQDVSDTIAAAINQEMFTRNY 655
           PPLV+AYALAG+MD D    PLGQD +G +V+++DIWP+  ++ + +A+AI  +MF   Y
Sbjct: 595 PPLVVAYALAGSMDVDLFNDPLGQDTEGNDVYMKDIWPTSAEIEEVVASAITSDMFDDGY 654

Query: 656 ADVFKGDDRWRNLPTPSGNTFEWDPNSTYVRKPPYFEGMTAKPEPVGNISGARVLALLGD 715
           ADVF GD++WR+LPTP G TFEWD  STYVRKPPYF+GM  +PEPV +I GARVL  LGD
Sbjct: 655 ADVFAGDEQWRSLPTPEGKTFEWDAESTYVRKPPYFDGMPQEPEPVTDIDGARVLLKLGD 714

Query: 716 SVTTDHISPAGAIKPGTPAARYLDEHGVDRKDYNSFGSRRGNHEVMIRGTFANIRLRNQL 775
           SVTTDHISPAGAIK  +PA  YL EHGV+++D+NS+GSRRGNHEVMIRGTFANIRLRNQ+
Sbjct: 715 SVTTDHISPAGAIKKDSPAGHYLAEHGVEQRDFNSYGSRRGNHEVMIRGTFANIRLRNQM 774

Query: 776 LDDVSGGYTRDFTQPGGPQAFIYDAAQNYAAQHIPLVVFGGKEYGSGSSRDWAAKGTLLL 835
                GG+TR           +++A++ Y A  +PLVV  GKEYGSGSSRDWAAKGT LL
Sbjct: 775 APGTEGGFTRYLDGGEDSVTSVFEASEKYIAAGVPLVVLAGKEYGSGSSRDWAAKGTALL 834

Query: 836 GVRAVIAESFERIHRSNLIGMGVIPLQFPEGKSASSLGLDGTEVFDITGIDVLNDGKTPK 895
           GV+AVIAES+ERIHRSNLIGMGV+PLQ+PEG+SA SLGL G E F ++G+  LNDG TP+
Sbjct: 835 GVKAVIAESYERIHRSNLIGMGVLPLQYPEGESAESLGLTGEETFSVSGVTELNDGTTPR 894

Query: 896 TVCVQATKGDGATIEFDAVVRIDTPGEADYYRNGGILQYVLRNILK 941
           TV V A   DG  +EFDAVVRIDTPGEA+YYRNGGI+QYVLRN+L+
Sbjct: 895 TVKVTA---DG--VEFDAVVRIDTPGEANYYRNGGIMQYVLRNLLR 935


Lambda     K      H
   0.316    0.136    0.403 

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: 2663
Number of extensions: 128
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: 943
Length of database: 936
Length adjustment: 44
Effective length of query: 899
Effective length of database: 892
Effective search space:   801908
Effective search space used:   801908
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