GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acnD in Marinobacter adhaerens HP15

Align 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) (EC 4.2.1.117) (characterized)
to candidate GFF3491 HP15_3433 aconitate hydratase 1

Query= BRENDA::Q8EJW3
         (867 letters)



>FitnessBrowser__Marino:GFF3491
          Length = 919

 Score =  717 bits (1850), Expect = 0.0
 Identities = 386/916 (42%), Positives = 553/916 (60%), Gaps = 64/916 (6%)

Query: 5   MNTQYRKPLPGTALDYFDTREAIEAIAPGAYAKLPYTSRVLAENLVRR-----CEPEMLT 59
           +NT       G    Y+   +A + +  G   +LP++ +VL ENL+R       +   + 
Sbjct: 11  LNTLSSLDAGGKTFHYYSLPKAADTL--GDLNRLPFSLKVLMENLLRNEDGTTVDRSHID 68

Query: 60  ASLKQIIESKQELDFPWFPARVVCHDILGQTALVDLAGLRDAIAAKGGDPAQVNPVVPTQ 119
           A ++ + +   + +  + PARV+  D  G   +VDLA +R+A+ A G DPA +NP+ P  
Sbjct: 69  AMVQWMKDRHSDTEIQFRPARVLMQDFTGVPGVVDLAAMREAVQAAGKDPAMINPLSPVD 128

Query: 120 LIVDHSLAVEYGGFDKDAFAKNRAIEDRRNEDRFHFINWTQKAFKNIDVIPQGNGIMHQI 179
           L++DHS+ V+  G D  +F  N AIE  RN++R+ F+ W Q+AF N  V+P G GI HQ+
Sbjct: 129 LVIDHSVMVDKFG-DASSFKDNVAIEMERNQERYEFLRWGQQAFDNFRVVPPGTGICHQV 187

Query: 180 NLERMSPVIHARNG----VAFPDTLVGTDSHTPHVDALGVIAIGVGGLEAESVMLGRASY 235
           NLE +   +  ++     +A+PDTLVGTDSHT  ++ LG++  GVGG+EAE+ MLG+   
Sbjct: 188 NLEYLGKTVWQKDQDGKTIAYPDTLVGTDSHTTMINGLGILGWGVGGIEAEAAMLGQPVS 247

Query: 236 MRLPDIIGVELTGKPQPGITATDIVLALTEFLRAQKVVSSYLEFFGEGAEALTLGDRATI 295
           M +P+++G ++TGK + GITATD+VL +TE LR + VV  ++EF+G+G + + + DRATI
Sbjct: 248 MLIPEVVGFKITGKLREGITATDLVLTVTEMLRKKGVVGKFVEFYGDGLKDMPVADRATI 307

Query: 296 SNMTPEFGATAAMFYIDQQTLDYLTLTGREAEQVKLVETYAKTAGLWSDDLKQAVYPRTL 355
           +NM PE+GAT   F +D+QT+ Y+ LTGRE EQ++LVE YAK  GLW +   + VY   L
Sbjct: 308 ANMAPEYGATCGFFPVDEQTIKYMRLTGREEEQLELVEAYAKAQGLWREPGHEPVYTDNL 367

Query: 356 HFDLSSVVRTIAGPSNPHARV------PTSELAARGISGEVEN----------------- 392
             D+  V  ++AGP  P  RV       + EL      G  EN                 
Sbjct: 368 ELDMGEVEASLAGPKRPQDRVALKNMKSSFELLMETAEGPAENREANLESEGGQTAVGVD 427

Query: 393 ---------------EPGLMPDGAVIIAAITSCTNTSNPRNVIAAGLLARNANAKGLTRK 437
                          E   +  GAV+IAAITSCTNTSNP  ++AAGL+A+ A  KGL+ K
Sbjct: 428 DSYKHHASQPLEMNGEKSRLDPGAVVIAAITSCTNTSNPSVMMAAGLIAQKAVQKGLSTK 487

Query: 438 PWVKTSLAPGSKAVQLYLEEANLLPELESLGFGIVGFACTTCNGMSGALDPVIQQEVIDR 497
           PWVKTSLAPGSK V  YL+      +L+ LGF +VG+ CTTC G SG L   +++ + D 
Sbjct: 488 PWVKTSLAPGSKVVTDYLKVGGFQDDLDKLGFNLVGYGCTTCIGNSGPLPDAVEKAISDG 547

Query: 498 DLYATAVLSGNRNFDGRIHPYAKQAFLASPPLVVAYAIAGTIRFDIEKDVLGLDKDGKPV 557
           DL   +VLSGNRNF+GR+HP  K  +LASPPLVVAYA+AG +R D+ +D LG DKDG PV
Sbjct: 548 DLTVASVLSGNRNFEGRVHPLVKTNWLASPPLVVAYALAGNVRLDLSQDPLGNDKDGNPV 607

Query: 558 RLINIWPSDAEIDAVIAASVKPEQFRKVYEPMFDLSVDYGD-KV--SPLYDWRPQSTYIR 614
            L ++WPS  EI A     VK + FRK Y  +FD    +   KV  S +Y+W  +STYI+
Sbjct: 608 YLKDLWPSQQEI-AEAVEKVKTDMFRKEYAEVFDGDATWKSIKVPESKVYEWSDKSTYIQ 666

Query: 615 RPPYWEGALAGERT---LKGMRPLAVLGDNITTDHLSPSNAIMMDSAAGEYLHKMGLPEE 671
            PP++EG          +K    LA+LGD++TTDH+SP+ +   D+ AG+YL + G+  +
Sbjct: 667 HPPFFEGLKEEPDAIDDIKDANILALLGDSVTTDHISPAGSFKPDTPAGKYLQEHGVEPK 726

Query: 672 DFNSYATHRGDHLTAQRATFANPKLKNEMAIVDGKVKQGSLARIEPEGIVTRMWEAIETY 731
           DFNSY + RG+H    R TFAN +++NEM  +DG   +G   +  P G    +++A   Y
Sbjct: 727 DFNSYGSRRGNHEVMMRGTFANVRIRNEM--LDG--VEGGYTKFVPTGEQMAIYDAAMKY 782

Query: 732 MDRKQPLIIIAGADYGQGSSRDWAAKGVRLAGVEAIVAEGFERIHRTNLVGMGVLPLEFK 791
            ++  PL++IAG +YG GSSRDWAAKG RL GV+A+VAE +ERIHR+NL+GMGV+PL+F 
Sbjct: 783 QEKGTPLVVIAGKEYGTGSSRDWAAKGTRLLGVKAVVAESYERIHRSNLIGMGVMPLQFP 842

Query: 792 AGENRATYGIDGTEVFDV---IGSIAPRADLTVIITRKNGERVEVPVTCRLDTAEEVSIY 848
            G +R +  + G E   +    G I P   L + +  K+G      +  R+DTA E   +
Sbjct: 843 EGTDRKSLKLTGEETISIEGLSGEIKPGQTLKMTVKYKDGSTETCELKSRIDTANEAVYF 902

Query: 849 EAGGVLQRFAQDFLES 864
           + GG+L    ++ L +
Sbjct: 903 KHGGILHYVVREMLRT 918


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: 2007
Number of extensions: 96
Number of successful extensions: 10
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 867
Length of database: 919
Length adjustment: 43
Effective length of query: 824
Effective length of database: 876
Effective search space:   721824
Effective search space used:   721824
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