GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaM in Marinobacter adhaerens HP15

Align PEP-dependent dihydroxyacetone kinase, phosphoryl donor subunit DhaM; Dihydroxyacetone kinase subunit M; EC 2.7.1.121 (characterized)
to candidate GFF3781 HP15_3723 PTS system, glucose-specific EIIA/HPr/phosphoenolpyruvate-protein phosphotransferase components

Query= SwissProt::D4GL26
         (473 letters)



>FitnessBrowser__Marino:GFF3781
          Length = 978

 Score =  134 bits (338), Expect = 1e-35
 Identities = 114/380 (30%), Positives = 173/380 (45%), Gaps = 35/380 (9%)

Query: 111 AAAGADIDTVIDVAMNALAAKQAQLGITPPAHAASLPAQAPDSDARSVTVTIRNHHGLHV 170
           A  G +   +++     LA  +   G++  A  A L  +A  +DA +  VT+ N HGLH 
Sbjct: 267 AGPGDECHDLLERIDTFLAGDEPIQGLSAEALLARLSGEA--ADAVTAKVTLLNTHGLHA 324

Query: 171 RPASRLVAALAGMNADL---VLEKQGQCVKPDSLNQIALLQVRCHDAVTLSASGPDAERA 227
           RPA +LV      NA +   +LE +G  V   SL ++  L  R    + LSA+G DA +A
Sbjct: 325 RPAKQLVQEARRHNASIRLRLLEGEGAAVSATSLTRVIGLGARRGQTLLLSATGDDASQA 384

Query: 228 LAAFESLAAEDFGEHPESMALKTSASTV-EKVQGKAVFYPLPLAQPARHP---------- 276
           + +  S      GE    +      + V E  Q  A+    P+   A  P          
Sbjct: 385 IQSLTSAIEGGLGEKVSPLRSADPQTKVPEAEQAPALTDDQPVKAVAASPGLALAPAFVM 444

Query: 277 ----------CSDVGQEERRLQQAIVDTLNDLNALAALAEKKYGASVAAIFSGHYTLLDD 326
                       D  Q+ +RL QA+      L  L   AE   G   A I S H  +L D
Sbjct: 445 RQPTLEYPQFAEDSEQQIQRLNQAVDSADGQLRTLIRQAE---GGEAAPILSVHVEMLQD 501

Query: 327 PDLFDAACKVIRNDSCCAESAWYQVLMELSQQYQHLDDAYLQARFIDIEDILYRSLCHLK 386
            DL+ A  + I N+   AE+ W++ +   ++  + L D  L  R  D+ D+  R L +L 
Sbjct: 502 EDLYQATLEAI-NEGASAEAGWWKAIDTAARGQEALADRLLAERAADLRDVGRRVLSNLC 560

Query: 387 GRDIRLPTP-DVPAIIVADDIFPSAVVNLNAQLVKGICLREGSTLSHAAIIAQQAGIAFI 445
           G  + +PTP D P I+VADD+ PS V  L+   V+G+    G   SH+AI+A+  G+  +
Sbjct: 561 G--VAMPTPPDTPYILVADDLGPSDVARLDTTRVRGLVTARGGATSHSAILARALGLPAV 618

Query: 446 CQQG-AVLDIIQPEDRLLID 464
              G  +L I+   D L++D
Sbjct: 619 VGTGERILTILNGSD-LVVD 637


Lambda     K      H
   0.320    0.133    0.380 

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: 959
Number of extensions: 30
Number of successful extensions: 3
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: 473
Length of database: 978
Length adjustment: 39
Effective length of query: 434
Effective length of database: 939
Effective search space:   407526
Effective search space used:   407526
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 (21.8 bits)
S2: 54 (25.4 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