GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfQ in Collimonas arenae Ter10

Align Galactofuranose-binding protein YtfQ (characterized)
to candidate WP_061533690.1 CAter10_RS12705 ABC transporter substrate-binding protein

Query= SwissProt::P39325
         (318 letters)



>NCBI__GCF_001584165.1:WP_061533690.1
          Length = 322

 Score =  305 bits (780), Expect = 1e-87
 Identities = 164/306 (53%), Positives = 218/306 (71%), Gaps = 8/306 (2%)

Query: 13  AAMSSMALAAPLTVGFSQVGSESGWRAAETNVAKSEAEKRGITLKIADGQQKQENQIKAV 72
           AA SS     PL +GFSQVG+ES WR A T   K  A++ G+TLK AD QQKQENQ+KA+
Sbjct: 20  AAASSAFADKPLVLGFSQVGAESEWRTANTASIKDAAKQAGVTLKFADAQQKQENQVKAI 79

Query: 73  RSFVAQGVDAIFIAPVVATGWEPVLKEAKDAEIPVFLLDRSIDVKDKSLYMTTVTADNIL 132
           RSF+AQ VD I  +PVV +GW+ VL+EAK A+IPV L DR+++V DKSLY+T + +D + 
Sbjct: 80  RSFIAQKVDVIAFSPVVESGWDTVLREAKAAKIPVILTDRAVNVSDKSLYVTFIGSDFVE 139

Query: 133 EGKLIGDWLVKEVNGKPC---NVVELQGTVGASVAIDRKKGFAEAIKNAPNIKIIRSQSG 189
           EG+  G WL++     P    N+VELQGTVG++ AIDRK GFAE I   P++KIIRSQ+G
Sbjct: 140 EGRRAGRWLLERAKTMPAGDINIVELQGTVGSAPAIDRKAGFAETIAANPHLKIIRSQTG 199

Query: 190 DFTRSKGKEVMESFIKAENNGKNICMVYAHNDDMVIGAIQAIKEAGLKPGKDILTGSIDG 249
           DFTR+KGKEVME+F+K +  GK I ++YAHNDDM IGAIQAI+EAGLKPG DIL  S+DG
Sbjct: 200 DFTRAKGKEVMEAFLKTD--GKKINVLYAHNDDMAIGAIQAIEEAGLKPGVDILVISVDG 257

Query: 250 VPDIYKAMMDGEANASVELTPNMAGPAFDALEKYKKDG-TMPEKLTLTKSTLYLPDTAKE 308
           V   ++AMM G+ N +VE +P + GP    + K    G T+P+++T T+  ++  + A +
Sbjct: 258 VKGAFEAMMAGKLNVTVECSP-LLGPQLMKIAKQVVAGETVPKRIT-TEEGVFPAEVAAK 315

Query: 309 ELEKKK 314
           E   +K
Sbjct: 316 EFPNRK 321


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: 291
Number of extensions: 9
Number of successful extensions: 3
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: 322
Length adjustment: 28
Effective length of query: 290
Effective length of database: 294
Effective search space:    85260
Effective search space used:    85260
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