GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfQ in Rhizobium freirei PRF 81

Align Galactofuranose-binding protein YtfQ (characterized)
to candidate WP_004118879.1 RHSP_RS15695 ABC transporter substrate-binding protein

Query= SwissProt::P39325
         (318 letters)



>NCBI__GCF_000359745.1:WP_004118879.1
          Length = 320

 Score =  413 bits (1061), Expect = e-120
 Identities = 210/315 (66%), Positives = 251/315 (79%), Gaps = 2/315 (0%)

Query: 5   LLIVSAVSAAMSSMALAAPLTVGFSQVGSESGWRAAETNVAKSEAEKRGITLKIADGQQK 64
           L+  +  +A M + A A  L VGFSQ+GSESGWRAAET + K EA+KRGI LK AD QQK
Sbjct: 7   LISATIFAACMFTSASAKQLVVGFSQIGSESGWRAAETTLTKQEAKKRGIDLKFADAQQK 66

Query: 65  QENQIKAVRSFVAQGVDAIFIAPVVATGWEPVLKEAKDAEIPVFLLDRSIDVKDKSLYMT 124
           QENQIKA+RSF+AQGVDAI +APVV TGW+ VLKEAK+A+IPV LLDR+++   K LY+T
Sbjct: 67  QENQIKAIRSFIAQGVDAILLAPVVETGWDAVLKEAKEAKIPVILLDRTVN-GPKDLYLT 125

Query: 125 TVTADNILEGKLIGDWLVKEVNGKPCNVVELQGTVGASVAIDRKKGFAEAIKNAPNIKII 184
            VT+D + EGK+ GDWLVK V  K CN+VELQGT G+S AI RKKGF EA+K   N+KI+
Sbjct: 126 AVTSDLVHEGKVAGDWLVKTVGDKKCNIVELQGTTGSSPAIARKKGFEEAVKGHDNLKIV 185

Query: 185 RSQSGDFTRSKGKEVMESFIKAENNGKNICMVYAHNDDMVIGAIQAIKEAGLKPGKDILT 244
           RSQ+GDFTR+KGKEVMESF+KAEN GKNIC +YAHNDDM +GAIQAIKEAGLKPGKDILT
Sbjct: 186 RSQTGDFTRAKGKEVMESFLKAENGGKNICALYAHNDDMAVGAIQAIKEAGLKPGKDILT 245

Query: 245 GSIDGVPDIYKAMMDGEANASVELTPNMAGPAFDALEKYKKDGTMPEKLTLTKSTLYL-P 303
            SID VPD++KAM  GEANA+VELTPNMAGPAFDAL+ Y K    P+K   T+S LY   
Sbjct: 246 VSIDSVPDLFKAMAAGEANATVELTPNMAGPAFDALDAYLKTKKEPQKWIQTESKLYTQA 305

Query: 304 DTAKEELEKKKNMGY 318
           D  ++  E+KK++GY
Sbjct: 306 DDPQKVYEQKKDLGY 320


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: 345
Number of extensions: 11
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: 318
Length of database: 320
Length adjustment: 28
Effective length of query: 290
Effective length of database: 292
Effective search space:    84680
Effective search space used:    84680
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