GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nupC' in Paraburkholderia bryophila 376MFSha3.1

Align RnsD, component of The (deoxy)ribonucleoside permease; probably takes up all deoxy- and ribonucleosides (cytidine, uridine, adenosine and toxic analogues, fluorocytidine and fluorouridine tested), but not ribose or nucleobases (characterized)
to candidate H281DRAFT_02963 H281DRAFT_02963 nucleoside ABC transporter membrane protein

Query= TCDB::Q8DU39
         (318 letters)



>FitnessBrowser__Burk376:H281DRAFT_02963
          Length = 305

 Score =  140 bits (354), Expect = 3e-38
 Identities = 99/311 (31%), Positives = 158/311 (50%), Gaps = 15/311 (4%)

Query: 1   MSLENMLALLISSMLVYATPLIFTSIGGVFSERSGVVNVGLEGIMVMGAFAGVVFNIEFA 60
           M+LE +LA+   + +  A P++  S G + SER+GV+N+ +EG+M+ GAF G  F     
Sbjct: 1   MNLE-LLAVFAGASIRLAAPMMLASTGELVSERAGVLNMSVEGMMLTGAFLGATF----- 54

Query: 61  HSFGKATPWIAALVGGLVGLLFSLLHALATINFRADHIVSGTVLNLLAPSLAVFFVKALY 120
            S+    P I  L G L  +  +LL A  ++  RA+ IV+G  +N+LA        + ++
Sbjct: 55  -SWLTGNPVIGLLCGMLGVIPLALLQAFLSVTMRANQIVTGIGINILALGGTTLAYRKIF 113

Query: 121 NKGQTDNISQSFGKFDFPILSHIPFLG-PIFFQGTSLVAYLAVLFSVFAWFILTKTKFGL 179
            + ++  +      +  P+L  IP LG P+F Q   L A LAVL       ++ +T  G+
Sbjct: 114 GE-RSSAVIPGLAHWSPPVLGKIPVLGEPVFGQVWLLYAGLAVLIGTSV--VMRRTALGV 170

Query: 180 RLRSVGEHPQAADTLGINVYLMRYLGVMISGLLGGIGGAIYAQSISVNFAGTTILGPGFI 239
            L + G  P+A D  G+ V  +RY  V+ SG++    G   +      F      G G++
Sbjct: 171 ALHATGVAPRAVDQSGLGVARLRYGAVVFSGVMSAAAGCFLSIGDIHTFTEGMTNGAGYL 230

Query: 240 ALAAMIFGKWNPIGAMLSSLFFGLSQSLAVIGGQLP-FLSKIPTVYLQIAPYALTILVLA 298
           A+AA+IFG W      L+ L FG + ++     QLP F   +PT  L + PY L ++ +A
Sbjct: 231 AIAAIIFGNWKVGRTALACLLFGAATAMQF---QLPMFGLHVPTALLIMLPYLLALVAVA 287

Query: 299 VFFGQAVAPKA 309
              G+  AP A
Sbjct: 288 GLIGRQSAPPA 298


Lambda     K      H
   0.328    0.143    0.422 

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: 267
Number of extensions: 13
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: 318
Length of database: 305
Length adjustment: 27
Effective length of query: 291
Effective length of database: 278
Effective search space:    80898
Effective search space used:    80898
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