GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Nocardioides daejeonensis MJ31

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate WP_110206994.1 DNK54_RS11055 ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>NCBI__GCF_003194585.1:WP_110206994.1
          Length = 368

 Score =  261 bits (666), Expect = 3e-74
 Identities = 152/369 (41%), Positives = 219/369 (59%), Gaps = 14/369 (3%)

Query: 10  AKTRKALTPL-LEIRNLTKSYDGQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGF 68
           A T++ LT   +E+  + K Y     ++D+ L I  GE   LLGASG GKSTLL ++AGF
Sbjct: 5   ANTQEPLTGASIEVDRIRKVYGSTTILNDIDLDIRAGEFLTLLGASGSGKSTLLNIIAGF 64

Query: 69  EQPSAGQIMLDGVDLSQVPPYLRPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIAS 128
            +   G + +DG  ++ VP + R + M+FQ YALFPHM+V  N+A+GL++   PKAEI  
Sbjct: 65  IKADGGDVRVDGKSITSVPAHKRGLGMVFQHYALFPHMSVYDNVAYGLRRHGFPKAEIPG 124

Query: 129 RVNEMLGLVHMQEFAKRKPHQLSGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRM 188
            V + L +V M    KR+P +LSGGQ+QRVALAR++  RP++LL+DEP+GALDK LR+++
Sbjct: 125 LVADALEMVEMGHLGKRRPAELSGGQQQRVALARAVVFRPRVLLMDEPLGALDKMLREQL 184

Query: 189 QLEVVDILERVGVTCVMVTHDQEEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAE 248
           QLE+  + + +G+T V VTHDQEEA+TM+ RIA++ +G  VQ+G PEE+Y+ P+ RY+AE
Sbjct: 185 QLEIRRLHKEMGITFVFVTHDQEEALTMSDRIALLEKGDIVQLGTPEELYDAPSCRYAAE 244

Query: 249 FIGSVNVFEGVLKERQEDGLVLDSPGLVHPLKVDADASVVDNVPVHVALRPEKIMLC--E 306
           FIG  N+  G    R  D          H +   A    V      + +RPE++ +   +
Sbjct: 245 FIGVSNIMTG---SRAGDVFTDTRNQTTHKVSGGAADGTV------LMVRPERLRVSAGQ 295

Query: 307 EPPANGCNFAVGEVIHIAYLGDLSVYHVRLKSGQMISAQLQNAHRHRKGLPTWGDEVRLC 366
             PA   N     V    YLG     HVR  SG+ + A+ +   R   G+   G  V L 
Sbjct: 296 VGPAGHENALPAIVSDCVYLGSDRTVHVRTASGEEMVARTE-VPRTDDGIQP-GVPVTLT 353

Query: 367 WEVDSCVVL 375
           W ++   VL
Sbjct: 354 WNIEDARVL 362


Lambda     K      H
   0.321    0.137    0.400 

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: 383
Number of extensions: 18
Number of successful extensions: 2
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: 377
Length of database: 368
Length adjustment: 30
Effective length of query: 347
Effective length of database: 338
Effective search space:   117286
Effective search space used:   117286
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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