GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt2d in Herbaspirillum seropedicae SmR1

Align Mannitol 2-dehydrogenase; M2DH; MDH; EC 1.1.1.67 (uncharacterized)
to candidate HSERO_RS02215 HSERO_RS02215 D-arabinitol 4-dehydrogenase

Query= curated2:P33216
         (477 letters)



>FitnessBrowser__HerbieS:HSERO_RS02215
          Length = 477

 Score =  239 bits (610), Expect = 1e-67
 Identities = 154/406 (37%), Positives = 214/406 (52%), Gaps = 12/406 (2%)

Query: 1   MTRSVTRPSYDRK-ALTPGIVHIGVGNFHRAHQAVYLDDLFALGEGHDWAILGAGVRPTD 59
           MTR+ T    D   +LT   +HIG G+FHRAHQAVYL+ L   G    W +  A +R   
Sbjct: 1   MTRTATSIDQDAADSLT--WLHIGAGSFHRAHQAVYLNALRESGADRRWQLALANIRADM 58

Query: 60  ARMREALAAQDNLSTVIELDPAGHRARQVGAMVG-FLPVEADNAALIEAMSDPRIRIVSL 118
           + + EALA Q    T+  + P G R+ Q  A +G  LP +A    LI A ++ R RI+S 
Sbjct: 59  SPLLEALARQQGQYTLETVTPQGQRSYQRIASIGRILPWDAQLTQLIAAGAEERTRIISF 118

Query: 119 TVTEGGYYVDASGAFDPTHPDIVADAA----HPARPATAFGAILAALRARRDAGV-TPFT 173
           TVTEGGYY+D     D ++ D+  D          P T +GAI A L AR  A      T
Sbjct: 119 TVTEGGYYLDHQHQLDTSNADLAEDLRCALDGSGAPRTIYGAIAAILHARSQAHPQAALT 178

Query: 174 VMSCDNLPGNGHVTRNAVVGLAELY-DAELAGWVKAQVAFPNGMVDRITPA-TGPHEREL 231
           +++CDNL  NG   R+ +     L  +  L  W++A    PN MVDRITP  T    + +
Sbjct: 179 LLNCDNLRHNGERFRDGLRQFLTLRGETALVSWMQANTTSPNAMVDRITPRPTAAVAQRV 238

Query: 232 AQGFGLADPVPVTCEPFRQWVIEDHFPAGRPALEKVGVTFTPHVHAYEAMKIRILNGGHA 291
            +  G+ DP  +  E F QWVIED F AGRP LE+ GV     V  YE  KIRILN  H+
Sbjct: 239 KEATGIDDPCALMGESFIQWVIEDDFKAGRPRLEEAGVEMVQSVLPYEEAKIRILNASHS 298

Query: 292 VIAYPSALMDIQLVHAAMAHPLIAAFLHKVEVEEILPHVPPVPDTSIPDYLTLIESRFSN 351
            IA+   L  +Q +H       I    +    ++++  + P P   +  Y     +RFSN
Sbjct: 299 CIAWAGTLAGLQYIHEGTLRDDIRQMAYDYVTQDVIACLTPSP-IDLAAYRDTTLARFSN 357

Query: 352 PEIADTTRRLCLDGSNRQPKFIVPSLRDNLAAGTVPKGLVLLSALW 397
           P I DT +R+  DG ++ P FI P+L++++AAG  P+   +L AL+
Sbjct: 358 PAIQDTNQRVAADGYSKIPGFIRPTLQESMAAGRDPRATAMLPALF 403


Lambda     K      H
   0.321    0.136    0.418 

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: 519
Number of extensions: 33
Number of successful extensions: 6
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: 477
Length of database: 477
Length adjustment: 33
Effective length of query: 444
Effective length of database: 444
Effective search space:   197136
Effective search space used:   197136
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 51 (24.3 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