GapMind for catabolism of small carbon sources

 

Alignments for a candidate for cbtD in Herbaspirillum seropedicae SmR1

Align CbtD, component of Cellobiose and cellooligosaccharide porter (characterized)
to candidate HSERO_RS15940 HSERO_RS15940 peptide ABC transporter substrate-binding protein

Query= TCDB::Q97VF5
         (362 letters)



>FitnessBrowser__HerbieS:HSERO_RS15940
          Length = 334

 Score =  175 bits (444), Expect = 1e-48
 Identities = 101/302 (33%), Positives = 167/302 (55%), Gaps = 6/302 (1%)

Query: 44  MILEVHNLNVIYDEGNSRIIKAVNDVSFGVEKGEILGIIGESGSGKTTLISAILRAIRPP 103
           ++L+V NL V     N  ++ AV  + F V +GE+L ++GESG GK+    A++  +   
Sbjct: 3   VLLDVKNLKVDLPTENG-MLHAVRGIDFQVRRGEMLCLVGESGCGKSMTSLALMGLLPRK 61

Query: 104 GKIISGKVIFNGMDIFSMTIDEFRKLLWKDISYVPQASQNALNPVLPISEIFYHEAISHG 163
            +  +  ++F+G+D+  M   +  +L  K ++ + Q    +LNP   +        +   
Sbjct: 62  AQCSADHILFDGVDLHGMPDKQLMQLRGKRMAMIFQEPMTSLNPSYTLGNQLCEAMLQQP 121

Query: 164 EADKKRVIERASELLKLVGLDPARV-LKMYPFQLSGGMKQRVMIALSLLLNPKLILMDEP 222
              +    ERA  LL   G+  A   L+ YP QLSGG++QRVMIA+SL+ NP LI+ DEP
Sbjct: 122 GVSRAEARERALYLLHRTGISNAEDRLRQYPHQLSGGLRQRVMIAMSLMCNPDLIIADEP 181

Query: 223 TSALDMLNQELLLKLIKNINQEMGVTIVYVTHDILNIAQIANRLLVMYKGYVMEEGKTEE 282
           T+ALD+  Q  +L++I+ + QE G  ++++THD+  +++IA+R+ VMY G V+E     +
Sbjct: 182 TTALDVTIQAQILRMIRELQQEFGAAVIFITHDLGVVSRIADRVAVMYAGQVVETTDVAQ 241

Query: 283 IIKSPLNPYTSLLVSSIP----SLKGEVKVINVPLDEPLVSKEKGCPFLARCSKAFGRCK 338
           +   P +PYT  L++ IP    +L G        +   LV +  GC F  RC+KA   C+
Sbjct: 242 LFAQPRHPYTQGLLNCIPVRGKTLPGSHLQAIPGVVPSLVGQVSGCAFRNRCAKADSGCE 301

Query: 339 EE 340
            +
Sbjct: 302 RD 303


Lambda     K      H
   0.319    0.138    0.391 

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: 245
Number of extensions: 10
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: 362
Length of database: 334
Length adjustment: 29
Effective length of query: 333
Effective length of database: 305
Effective search space:   101565
Effective search space used:   101565
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: 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