GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoxyribonate-transport in Cupriavidus basilensis 4G11

Align 2-deoxy-D-ribonate transporter 1 (characterized)
to candidate RR42_RS04270 RR42_RS04270 MFS transporter

Query= reanno::WCS417:GFF1429
         (438 letters)



>FitnessBrowser__Cup4G11:RR42_RS04270
          Length = 434

 Score =  306 bits (785), Expect = 6e-88
 Identities = 166/401 (41%), Positives = 242/401 (60%), Gaps = 9/401 (2%)

Query: 19  VKLMPLLIIAYILSFLDRTNIALAKHHLDVDLGISAAAYGLGAGLFFLTYALSEIPSNLI 78
           ++L+P L++ Y++++LDR N+  AK  +  DL  S   YGLGAG+FF+ Y L E+PSN+I
Sbjct: 25  LRLVPFLLLCYVVAYLDRVNVGFAKLQMLGDLKFSETIYGLGAGIFFIGYFLFEVPSNVI 84

Query: 79  MHKVGARFWIARIMVTWGLISAAMAFVQGETSFYVLRLLLGIAEAGLFPGVMLYLTYWFN 138
           +HKVGAR WIARIM+TWG+ISAAM FV   T FYVLR LLGIAEAG FPG++LYLTYW+ 
Sbjct: 85  LHKVGARIWIARIMITWGVISAAMMFVTTPTMFYVLRFLLGIAEAGFFPGIILYLTYWYP 144

Query: 139 REQRARATGYFLLGVCFANIIGGPVGAALMR-MDGMLGWHGWQWMFMLEGLPAVAFAWVV 197
             +R R T +F+  +  + +IGGP+   +M+  DG  GW GWQWMF+LEG+P+V    VV
Sbjct: 145 SHRRGRTTTFFMTAIALSGVIGGPLSGWMMQSFDGRNGWSGWQWMFLLEGIPSVLVGLVV 204

Query: 198 WRKLPDRPSKAPWLSAEEARGIEQRIAQET--EEGAGEGGHSLKNWLTPQILLAIFVYFC 255
              L DR   A WLS EE   +++ IA E   +E A  G    K   +P++ L   +YF 
Sbjct: 205 LAYLDDRIVHAKWLSNEEKALLQRNIAAEDMHKEDAPIG----KVLSSPRVWLMSAIYFS 260

Query: 256 HQITIYTVIFFLPSIISKYGELSTMSVGLLTSLPWIAAALGALLIPRFA-TTPGRCRRLL 314
             + +Y V F+LP+II + G  S + +GLLT++P+  A  G +L+   A  T  R   + 
Sbjct: 261 FVMGLYGVSFWLPTIIKQTGVKSPLDIGLLTAIPYGCAVAGMVLVAYSADRTRERRWHIA 320

Query: 315 VTGLL-TMALGLGIASVSGPVFSLLGFCLSAVMFFVVQSIIFLYPASRLKGVALAGGLGF 373
           +  LL  + L L +   +  V +LLG  L+ +       + +  P + L G   A G+  
Sbjct: 321 IPALLGAVGLVLSVQWHNNTVLALLGLTLATIGILTTLPLFWSLPTAFLAGTGAAAGIAL 380

Query: 374 VNACGLLGGFVGPSVMGVIEQSTGNAMNGLKVIALVLVVAA 414
           +N+ G L GF+ P  +G ++  T +  +G+ ++A  LV  A
Sbjct: 381 INSLGNLAGFISPYAVGWLKDMTQSTDSGMYLLAACLVAGA 421


Lambda     K      H
   0.327    0.141    0.438 

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: 581
Number of extensions: 22
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: 438
Length of database: 434
Length adjustment: 32
Effective length of query: 406
Effective length of database: 402
Effective search space:   163212
Effective search space used:   163212
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: 51 (24.3 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