GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfQ in Gallaecimonas xiamenensis 3-C-1

Align Galactofuranose-binding protein YtfQ (characterized)
to candidate WP_156804529.1 B3C1_RS10875 substrate-binding domain-containing protein

Query= SwissProt::P39325
         (318 letters)



>NCBI__GCF_000299915.1:WP_156804529.1
          Length = 309

 Score =  330 bits (846), Expect = 3e-95
 Identities = 174/301 (57%), Positives = 222/301 (73%), Gaps = 5/301 (1%)

Query: 14  AMSSMALAAPLTVGFSQVGSESGWRAAETNVAKSEAEKRGITLKIADGQQKQENQIKAVR 73
           A+S  ALA  +TVGFSQVGSESGWR++ +   K EA+ RGI LK ADGQQKQENQI+AVR
Sbjct: 14  ALSHSALA--ITVGFSQVGSESGWRSSFSQDMKDEAKSRGIDLKFADGQQKQENQIRAVR 71

Query: 74  SFVAQGVDAIFIAPVVATGWEPVLKEAKDAEIPVFLLDRSIDVKDKSLYMTTVTADNILE 133
           SF+AQGVDAI IAPVV TGW PVLKEAK A IPV +LDR+I   +  LY+T + +D   E
Sbjct: 72  SFIAQGVDAIIIAPVVETGWTPVLKEAKRARIPVVILDRNIKAAE-GLYVTRIASDFTEE 130

Query: 134 GKLIGDWLVKEVNGKPCNVVELQGTVGASVAIDRKKGFAEAIKNAPNIKIIRSQSGDFTR 193
           G+    WL+ +  G+ CN+VELQGTVGA+ AIDR KGF E I   P  KI+RSQ+ +FTR
Sbjct: 131 GRKAARWLMDKTKGQ-CNIVELQGTVGATAAIDRAKGFNEVIGAYPQAKIVRSQTAEFTR 189

Query: 194 SKGKEVMESFIKAENNGKNICMVYAHNDDMVIGAIQAIKEAGLKPGKDILTGSIDGVPDI 253
           +KGKEVMESF+KAE + +++C +++HND+M +GAIQAIKEAGLKPGKD+L  S+DGVPD 
Sbjct: 190 AKGKEVMESFLKAE-DPQSLCALWSHNDEMALGAIQAIKEAGLKPGKDLLVVSVDGVPDY 248

Query: 254 YKAMMDGEANASVELTPNMAGPAFDALEKYKKDGTMPEKLTLTKSTLYLPDTAKEELEKK 313
           +KAM +G+AN +VEL P++  PA+  +EK         KL  T   ++  DTA  E +K+
Sbjct: 249 FKAMAEGDANITVELNPHLGAPAYQVVEKVLAGDKGIPKLISTTGEVFGQDTAATEYQKR 308

Query: 314 K 314
           K
Sbjct: 309 K 309


Lambda     K      H
   0.313    0.130    0.363 

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: 304
Number of extensions: 10
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: 309
Length adjustment: 27
Effective length of query: 291
Effective length of database: 282
Effective search space:    82062
Effective search space used:    82062
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 48 (23.1 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