GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malF_Aa in Phaeobacter inhibens BS107

Align Binding-protein-dependent transport systems inner membrane component (characterized, see rationale)
to candidate GFF1647 PGA1_c16700 binding protein-dependent transport system, inner membrane component

Query= uniprot:C8WUR0
         (321 letters)



>FitnessBrowser__Phaeo:GFF1647
          Length = 316

 Score =  133 bits (334), Expect = 6e-36
 Identities = 101/322 (31%), Positives = 160/322 (49%), Gaps = 48/322 (14%)

Query: 12  GRERAKRRVDWV----AYGYLSPALVTICVLSILPIFYTIYISFTNFNQMHFLSYQFVGL 67
           G   A+R + W      + YLSP ++ I  + ++P+   I  SF +   ++  +  +VG 
Sbjct: 17  GGTGARRSLYWQYMVEPFLYLSPMILLIGSVMLIPLIVGISYSFQSIELLNPFATGWVGF 76

Query: 68  KNYEELLNPHD---PLSNLFLPTFIWTLVYALCTTALAYLVGLFLAVLLNNKHMRERTLY 124
           +NYE+L +       L N F  TF W++ +        + +GL LA+LLN +   ++ L+
Sbjct: 77  ENYEKLWSDRKFWIALENTFFWTF-WSIFFQ-------FFLGLGLAMLLNTQFFGKK-LF 127

Query: 125 RTLLIVPWAVPNLISMLAWQGLLNDQYGQINALL---------HGVFGLPRIPWLTSALW 175
           + L+ +PWAVP  +S L W  L N   G I   L         + + G P +     A+W
Sbjct: 128 QALVFLPWAVPTFLSALTWAWLFNPVIGPIPHWLAALGVLSEPYNILGDPDL-----AIW 182

Query: 176 ARIAVIMVNVWAGFPYMMTVCLGALQSIPTDQYEAAEIDGANWWQVFRYVTMPSVWRISL 235
             I     N+W G P+     L ALQSIP + YEAAEIDGA  WQ F  +T+P +  +  
Sbjct: 183 GPITA---NIWFGVPFFAITLLAALQSIPGELYEAAEIDGATPWQSFTKITLPFLAPMIA 239

Query: 236 PLLIPSFSYNFNNFNASYLLTGGGPPNSNNPFLGQTDILATAAYKMTLTFNRYDLG--AT 293
             ++    +  N  +  +++TGGGP NS       T IL+T  Y  T  F + D G  +T
Sbjct: 240 ITVMLRTIWIANFADLIFVMTGGGPANS-------TQILST--YIFTTAFRKLDFGYAST 290

Query: 294 ISVLLFILV----ALISWVQMR 311
           I+V L I++     ++ W++ R
Sbjct: 291 IAVALLIILLAYAVILLWMRKR 312


Lambda     K      H
   0.327    0.140    0.451 

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: 369
Number of extensions: 20
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: 321
Length of database: 316
Length adjustment: 27
Effective length of query: 294
Effective length of database: 289
Effective search space:    84966
Effective search space used:    84966
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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