GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5403 in Rhodococcus qingshengii djl-6-2

Align ABC transporter for D-Alanine, permease component 2 (characterized)
to candidate WP_050656521.1 C1M55_RS16560 amino acid ABC transporter permease

Query= reanno::pseudo6_N2E2:Pf6N2E2_5403
         (375 letters)



>NCBI__GCF_002893965.1:WP_050656521.1
          Length = 318

 Score = 82.8 bits (203), Expect = 1e-20
 Identities = 66/219 (30%), Positives = 114/219 (52%), Gaps = 11/219 (5%)

Query: 160 VAEGFWPFVISVVLAIVA-IVLMTRWANKRFEATGEPFHKFWVGLALFLVIPALSALLFG 218
           +++  W  +   +L++ A IVL    A  R           WV L +F   P    L+F 
Sbjct: 62  ISKAAWVTIQLTILSMAAAIVLGIVLAVMRLSPNPVLKSAAWVYLWVFRGTPVYVQLVFW 121

Query: 219 A--PVHWEMPELKGFNFVGGWV------LIPELLALTLALTVYTAAFIAEIVRSGIKSVS 270
              P  ++  +L G  FV  +V      L    L   + L +  AA++AEIVR+GI SV+
Sbjct: 122 GLFPSIYKSIDL-GVPFVHQFVHFDMQDLQAAFLFAVIGLALNEAAYMAEIVRAGIASVN 180

Query: 271 HGQTEAARSLGLRNGPTLRKVIIPQALRVIIPPLTSQYLNLAKNSSLAAGIGYPEMVSLF 330
            GQTEA+ +LG+  G T+R+ ++PQA+RVIIPP  ++ ++L K +SL   +     +   
Sbjct: 181 EGQTEASVALGMTWGQTMRRTVLPQAMRVIIPPTGNELISLLKTTSLVTAVPLSTELYGR 240

Query: 331 AGTVLNQTGQAIEVIAITMSVYLAISISISLLMNWYNKR 369
           A  +     + I ++ + ++ YLA++ S+ ++  +Y +R
Sbjct: 241 ARDISGANFEPIPLLMVAVTWYLAMT-SVLMVGQYYVER 278



 Score = 47.4 bits (111), Expect = 6e-10
 Identities = 35/118 (29%), Positives = 58/118 (49%), Gaps = 22/118 (18%)

Query: 8   VVTVVAVIALGWFLFDNTQTNLQHRGITSGFGFLERSAGFGIAQHLIDYTEADSYARVFL 67
           V  VV V+ +G F++ +  TN Q       FG+          Q+L D    D  ++   
Sbjct: 26  VAAVVVVVLVGLFIYGSA-TNEQ-------FGWAT------YRQYLFD----DRISKAAW 67

Query: 68  IGLLNTLLVTFIGVILATILGFIIGVARLSQNWIISKLATVYVEVFRNIPPLLQILFW 125
           +    T+ +T + +  A +LG ++ V RLS N ++   A VY+ VFR  P  +Q++FW
Sbjct: 68  V----TIQLTILSMAAAIVLGIVLAVMRLSPNPVLKSAAWVYLWVFRGTPVYVQLVFW 121


Lambda     K      H
   0.328    0.141    0.430 

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: 265
Number of extensions: 12
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 375
Length of database: 318
Length adjustment: 29
Effective length of query: 346
Effective length of database: 289
Effective search space:    99994
Effective search space used:    99994
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 (21.8 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