GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acnD in Nocardioides dokdonensis FR1436

Align 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) (EC 4.2.1.117) (characterized)
to candidate WP_068112647.1 I601_RS17670 aconitate hydratase

Query= BRENDA::Q8EJW3
         (867 letters)



>NCBI__GCF_001653335.1:WP_068112647.1
          Length = 936

 Score =  679 bits (1752), Expect = 0.0
 Identities = 381/906 (42%), Positives = 527/906 (58%), Gaps = 86/906 (9%)

Query: 36  AKLPYTSRVLAENLVRRCEPEMLTASLKQII-------ESKQELDFPWFPARVVCHDILG 88
           A LP++ +VL ENL+R  +   +TA   + I       +  QE+ F   PARV+  D  G
Sbjct: 36  ASLPFSLKVLLENLLRTEDGSDITADDVKAIAGWDADADPSQEIQFT--PARVIMQDFTG 93

Query: 89  QTALVDLAGLRDAIAAKGGDPAQVNPVVPTQLIVDHSLAVEYGGFDKDAFAKNRAIEDRR 148
              +VDLA +R+A+A  GGDP ++NP+ P ++++DHS+  +  G   +AF +N  IE  R
Sbjct: 94  VPCVVDLATMREAMADLGGDPTKINPLAPAEMVIDHSVIADVFG-TPEAFGRNVEIEYER 152

Query: 149 NEDRFHFINWTQKAFKNIDVIPQGNGIMHQINLERMSPVIHAR--NGV--AFPDTLVGTD 204
           N +R+ F+ W Q AF +  V+P G GI+HQ+N+E ++  +  R  +GV  A+PDT VGTD
Sbjct: 153 NRERYQFLRWGQGAFDDFKVVPPGTGIVHQVNIEHLARTVFTREVDGVLQAYPDTCVGTD 212

Query: 205 SHTPHVDALGVIAIGVGGLEAESVMLGRASYMRLPDIIGVELTGKPQPGITATDIVLALT 264
           SHT  V+ +GV+  GVGG+EAE+ MLG+   M +P ++G +L G    G TATD+VL +T
Sbjct: 213 SHTTMVNGIGVVGWGVGGIEAEAAMLGQPVSMLIPRVVGFKLNGDLPEGATATDLVLTIT 272

Query: 265 EFLRAQKVVSSYLEFFGEGAEALTLGDRATISNMTPEFGATAAMFYIDQQTLDYLTLTGR 324
           E LR   VV  ++EF+G G   L L +RATI NM+PEFG+T A+F ID++T  YL LTGR
Sbjct: 273 EMLREHGVVGKFVEFYGPGVSVLPLANRATIGNMSPEFGSTIAVFPIDEETTKYLELTGR 332

Query: 325 EAEQVKLVETYAKTAGLWSDDLKQAVYPRTLHFDLSSVVRTIAG---------------- 368
             EQ+ LVE YAK  GLW D   +  +   L  DL++VV ++AG                
Sbjct: 333 TPEQIALVEAYAKEQGLWHDPDAEPRFSEKLELDLATVVPSLAGPKRPQDRVSLSEAKES 392

Query: 369 ---------------------------------PSNPHARVPTSE--LAARGISGEVENE 393
                                            P N H   P +    A  G  G   N 
Sbjct: 393 FRSALADYAEDTDAQETKGYDENVEESFPASDTPHNGHGEAPPNGHVAAGSGAGGRPRNP 452

Query: 394 PGL---------MPDGAVIIAAITSCTNTSNPRNVIAAGLLARNANAKGLTRKPWVKTSL 444
             +         +  GAV IAAITSCTNTSNP  +I A LLA+ A  KGL RKPWVKT+L
Sbjct: 453 AQVTLADGTSFELDHGAVTIAAITSCTNTSNPSVMIGAALLAKKAVEKGLERKPWVKTTL 512

Query: 445 APGSKAVQLYLEEANLLPELESLGFGIVGFACTTCNGMSGALDPVIQQEVIDRDLYATAV 504
           APGSK V  Y E++ L P L+ LGF +VG+ CTTC G SG L P + Q V D DL   +V
Sbjct: 513 APGSKVVSDYYEKSGLTPYLDKLGFNLVGYGCTTCIGNSGPLIPEVSQAVNDNDLAVVSV 572

Query: 505 LSGNRNFDGRIHPYAKQAFLASPPLVVAYAIAGTIRFDIEKDVLGLDKDGKPVRLINIWP 564
           LSGNRNF+GRI+P  K  +LASPPLVVAYA+AG++  D+  D LG D +G  V + +IWP
Sbjct: 573 LSGNRNFEGRINPDVKMNYLASPPLVVAYALAGSMDVDLFNDPLGQDTEGNDVYMKDIWP 632

Query: 565 SDAEIDAVIAASVKPEQFRKVYEPMFDLSVDYGDKVSP---LYDWRPQSTYIRRPPYWEG 621
           + AEI+ V+A+++  + F   Y  +F     +    +P    ++W  +STY+R+PPY++G
Sbjct: 633 TSAEIEEVVASAITSDMFDDGYADVFAGDEQWRSLPTPEGKTFEWDAESTYVRKPPYFDG 692

Query: 622 ALAGER---TLKGMRPLAVLGDNITTDHLSPSNAIMMDSAAGEYLHKMGLPEEDFNSYAT 678
                     + G R L  LGD++TTDH+SP+ AI  DS AG YL + G+ + DFNSY +
Sbjct: 693 MPQEPEPVTDIDGARVLLKLGDSVTTDHISPAGAIKKDSPAGHYLAEHGVEQRDFNSYGS 752

Query: 679 HRGDHLTAQRATFANPKLKNEMAIVDGKVKQGSLARI--EPEGIVTRMWEAIETYMDRKQ 736
            RG+H    R TFAN +L+N+MA       +G   R     E  VT ++EA E Y+    
Sbjct: 753 RRGNHEVMIRGTFANIRLRNQMA----PGTEGGFTRYLDGGEDSVTSVFEASEKYIAAGV 808

Query: 737 PLIIIAGADYGQGSSRDWAAKGVRLAGVEAIVAEGFERIHRTNLVGMGVLPLEFKAGENR 796
           PL+++AG +YG GSSRDWAAKG  L GV+A++AE +ERIHR+NL+GMGVLPL++  GE+ 
Sbjct: 809 PLVVLAGKEYGSGSSRDWAAKGTALLGVKAVIAESYERIHRSNLIGMGVLPLQYPEGESA 868

Query: 797 ATYGIDGTEVFDVIGSIAPRADLTVIITRKNGERVEVPVTCRLDTAEEVSIYEAGGVLQR 856
            + G+ G E F V G        T    +   + VE     R+DT  E + Y  GG++Q 
Sbjct: 869 ESLGLTGEETFSVSGVTELNDGTTPRTVKVTADGVEFDAVVRIDTPGEANYYRNGGIMQY 928

Query: 857 FAQDFL 862
             ++ L
Sbjct: 929 VLRNLL 934


Lambda     K      H
   0.318    0.136    0.397 

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: 2121
Number of extensions: 112
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 867
Length of database: 936
Length adjustment: 43
Effective length of query: 824
Effective length of database: 893
Effective search space:   735832
Effective search space used:   735832
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.

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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