GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Marinobacter adhaerens HP15

Align D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate GFF4004 HP15_3944 alcohol dehydrogenase zinc-binding domain protein

Query= BRENDA::P22144
         (363 letters)



>FitnessBrowser__Marino:GFF4004
          Length = 368

 Score =  112 bits (279), Expect = 2e-29
 Identities = 105/345 (30%), Positives = 162/345 (46%), Gaps = 34/345 (9%)

Query: 30  DVLVQVKKTGICGSDIHFYAHGRIGNFVLTKPMVLGHESAGTVVQVGKGVTSLKVGDNVA 89
           ++ +++   G+C SD+        G      P+VLGHE+AG VV+VG+GVT+ K GD+V 
Sbjct: 31  EITIKIAACGVCHSDLS----ATTGKIPYPPPLVLGHEAAGVVVEVGEGVTAFKEGDHVV 86

Query: 90  IEPGIPSRFSDEYKSGHYNLCPHMAFA------ATPNSK--EGEP----NPPGTLCKYFK 137
                      +   G   LC +   A       T  +K  +GEP       G + ++  
Sbjct: 87  STFISMCGKCSQCVRGRPVLCENARKAMFNLPDGTVRTKGADGEPLNVFGACGVMAEFAT 146

Query: 138 SPEDFLVKLPDHVSLELGALVE-PLSVGVHA-SKLGSVAFGDYVAVFGAGPVGLLAAAVA 195
              D  VK+ + V ++  ALV   +  GV A      +  G   AVFG G VGL A    
Sbjct: 147 MHVDNCVKVDETVPMQNAALVGCAVMTGVGAVFNTAKLEPGSRAAVFGIGGVGLNAIQGC 206

Query: 196 KTFGAKGVIVVDIFDNKLKMAKDIGAATHTFN-SKTGGSEELIKAFGGNVPNVVLECTGA 254
            T GA+ V+ VD    KL MAK+ G ATHT N ++   + + +K   G V +   EC GA
Sbjct: 207 VTAGAEMVVAVDSNPAKLAMAKEFG-ATHTVNINEVEDAAKAVKKMTGGV-DYAFECVGA 264

Query: 255 EPCIKLGVDAIAPGGRFVQVGNAAGPVSFPITVFAM--KELTLFGSFRYGF---NDYKTA 309
            P ++    ++  GG  V VG A       +T   +   E TL GS+       +D+   
Sbjct: 265 GPVVEQAYKSLGRGGTAVVVGVADPKDKTSLTTLTLPADERTLKGSWLGSARPQHDFPRI 324

Query: 310 VGIFDTNYQNGRENAPIDFEQLITHRYKFKDAIEAYDLVRAGKGA 354
           +G+    Y+ G+    +  ++L+T  Y  ++A +A+D + AGK A
Sbjct: 325 LGL----YKAGK----LKLDELVTRTYPIEEAAQAFDDMVAGKNA 361


Lambda     K      H
   0.318    0.138    0.411 

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: 343
Number of extensions: 23
Number of successful extensions: 4
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: 363
Length of database: 368
Length adjustment: 30
Effective length of query: 333
Effective length of database: 338
Effective search space:   112554
Effective search space used:   112554
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: 49 (23.5 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