GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Pseudovibrio axinellae Ad2

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_068009667.1 PsAD2_RS19325 ribose ABC transporter permease

Query= uniprot:D8J112
         (347 letters)



>NCBI__GCF_001623255.1:WP_068009667.1
          Length = 314

 Score =  238 bits (608), Expect = 1e-67
 Identities = 132/302 (43%), Positives = 192/302 (63%), Gaps = 15/302 (4%)

Query: 43  LLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVGTMMTFCAV 102
           L++++   SFA+ NF+ VDN+++IL+ T++N V+A+  T+VI+TSGIDLSVG+++ F   
Sbjct: 16  LIILMAAVSFANANFLGVDNMLNILRQTSINAVIAMGMTFVILTSGIDLSVGSILAFAGA 75

Query: 103 MAGVVLTNWGMPLPLGIA--AAIFFGALSGWISGMVIAKLKVPPFIATLGMMMLLKGLSL 160
           +   ++   GM  PL +A  A I  GA  G  SG++I+   V PFIATL  M +++G +L
Sbjct: 76  ICASLI---GMDTPLVVALFATIMVGAGLGATSGVIISYFNVQPFIATLVGMTMIRGATL 132

Query: 161 VISGTRPIYFND---TEGFSAIAQDSLIGDLIPSLPIPNAVLILFLVAIGASIILNKTVF 217
           V +  RP+        E F       + G       IP+ V+++ ++      IL++T F
Sbjct: 133 VYTQGRPVSTGSHDVAESFYQFGAGYIFG-------IPHPVILMIVIFAICWFILSQTRF 185

Query: 218 GRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASRLNSAQPALGQGYEL 277
           GRY +A+G NE   RLSG+ V   K+ VY  SGA+  +AG+I+ +RL SAQP  G GYEL
Sbjct: 186 GRYVYAIGGNENVARLSGINVKKVKILVYALSGALAALAGIILTARLESAQPTAGLGYEL 245

Query: 278 DAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEWQTVVTGVIIILAVY 337
           DAIAAVV+GGTSL+GG G + GTIIGA I+ VL N L IM V+  +Q +  G +I+LAV 
Sbjct: 246 DAIAAVVLGGTSLAGGKGRVFGTIIGALIIGVLNNALNIMDVSSYYQMIAKGAVILLAVV 305

Query: 338 LD 339
           +D
Sbjct: 306 VD 307


Lambda     K      H
   0.326    0.139    0.398 

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: 242
Number of extensions: 14
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: 347
Length of database: 314
Length adjustment: 28
Effective length of query: 319
Effective length of database: 286
Effective search space:    91234
Effective search space used:    91234
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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