GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ngcF in Phyllobacterium brassicacearum STM 196

Align NgcF, component of N-Acetylglucosamine/N,N'-diacetyl chitobiose porter (NgcK (C) not identified) (characterized)
to candidate WP_106713054.1 CU102_RS21025 sugar ABC transporter permease

Query= TCDB::Q8RJU9
         (308 letters)



>NCBI__GCF_003010955.1:WP_106713054.1
          Length = 342

 Score =  125 bits (313), Expect = 2e-33
 Identities = 91/299 (30%), Positives = 148/299 (49%), Gaps = 39/299 (13%)

Query: 12  FLAVPLGLYALLVVWPFIQSIYYSFTDWTGLS-PDFKTVGFDNYERMLD----------- 59
           FL   + ++ + V+ PF  +  YS T    L  PD   VG D Y R+ D           
Sbjct: 48  FLLPNMLIFGIFVLLPFFINFAYSMTGGAALFLPDRNFVGADQYARLFDCSNYLDPNSCA 107

Query: 60  DDIFWKSLQHSLLFALLLPVVTIGLALFFAFMINVGGRRRRGGPVITGVRGSGFYKIVYF 119
           +D FW ++ ++  F LL   + IG++L  A ++N              +R   F++ V+F
Sbjct: 108 EDTFWTAVGNTGWFVLLQVTLMIGVSLVTALILN------------RDLRARSFWRAVFF 155

Query: 120 FPQVLSIAIVALLFAFAYNPDSGAINSLLRGIGLGDVQP-VWLGDPDLALWCVMAVIVWS 178
           FP +LS  +V L++ +      G +N  L G+G    +P  WL D + +    + V +W+
Sbjct: 156 FPVLLSPVVVGLIWKWILQRQ-GLLNFGLYGLGF---EPHAWLNDRNWSFAAAVGVSIWA 211

Query: 179 TVGFFVVLFSAGMASIPADIYEAALLDGANRVTTFFRITLPLLWDTVQSGWVYMGILALG 238
            +GF+ ++  AG+ +IP D+YEAA +DG      F RITLPLL   +    V + +L   
Sbjct: 212 HMGFYTLILLAGLQAIPKDLYEAAEMDGTKPTRVFLRITLPLLAPNLLV--VIVLVLIRA 269

Query: 239 AESFAVVHIMTTGPGGPDYSTTVMVLYVYQKAF-----RDGQAAYATTI-GVALLIVTL 291
            + F  V+++T   GGP  ST  +  Y+Y+  F       G AA A+ + G  L+++TL
Sbjct: 270 VQIFDEVYVLT--GGGPGTSTLFLTQYIYETGFAAQLRNPGLAAAASILMGAVLVVLTL 326


Lambda     K      H
   0.330    0.145    0.458 

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: 288
Number of extensions: 20
Number of successful extensions: 5
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: 308
Length of database: 342
Length adjustment: 28
Effective length of query: 280
Effective length of database: 314
Effective search space:    87920
Effective search space used:    87920
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: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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