Align Glucose transport system permease protein aka TT_C0327, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized)
to candidate WP_011913554.1 PST_RS12260 sugar ABC transporter permease
Query= TCDB::Q72KX3 (369 letters) >NCBI__GCF_000013785.1:WP_011913554.1 Length = 305 Score = 120 bits (301), Expect = 5e-32 Identities = 80/228 (35%), Positives = 121/228 (53%), Gaps = 18/228 (7%) Query: 155 WLATREQVLVFDWNRLPFYTALVVGLVLLYVAYTAYREGERRRALW------GLASAGVL 208 W + +LVF L +L++G+VL + R R ++ + G Sbjct: 77 WWVASQNLLVF--GGLFIAISLIIGVVLAVLLDQRIRREGLIRTIYLYPMALSMIVTGTA 134 Query: 209 LLWAFAFGQGL-RLLPYPEVHGFSL--------ALVGVILAAVWQMSGYTMALYLAGLRG 259 W G GL +LL GF + +++AAVWQ SG+ MAL+LAGLR Sbjct: 135 WQWLLNPGLGLDKLLRDWGWEGFRFDWLVDPDRVIYCLVIAAVWQASGFVMALFLAGLRS 194 Query: 260 IPVEVLEAARVDGASEWQLFRRVIFPMLAPITLSAMIVLGHIALKIFDLVFAM-AGLDYA 318 + ++ AA+VDGAS ++ R++ P L P+ SA+++L HIA+K FDLV AM AG Sbjct: 195 VDQSIIRAAQVDGASLPTIYLRIVLPSLRPVFFSALMILAHIAIKSFDLVAAMTAGGPGY 254 Query: 319 PTDVPAIYMYLLAFRGNQFAKGAAIGILLLLLVAVVVVPYLATQLRKE 366 +D+PA++MY F Q GAA +L+L V ++VPYL ++LR + Sbjct: 255 SSDLPAMFMYAHTFTRGQMGLGAASAMLMLGAVMAIIVPYLYSELRSK 302 Score = 96.7 bits (239), Expect = 7e-25 Identities = 60/160 (37%), Positives = 91/160 (56%), Gaps = 11/160 (6%) Query: 4 RILAFLVLLPSVLAVGVFVYGFIGQNLWVSLTDWGKDPAQALALRPELRFVGLENYRELF 63 R L LVL PS+L V V Y +IG +S T+ P ++VGL+ Y+ L+ Sbjct: 21 RWLPKLVLAPSMLIVLVGFYAYIGWTFLLSFTN--------SRFMPSYKWVGLQQYQRLW 72 Query: 64 TGFVDVRFRQSVVNLIFFTLFFMAGSLGLGLLLALAVDKAPRGEGFFRTVFLFPMALSFV 123 + R+ + NL+ F F+A SL +G++LA+ +D+ R EG RT++L+PMALS + Sbjct: 73 D---NDRWWVASQNLLVFGGLFIAISLIIGVVLAVLLDQRIRREGLIRTIYLYPMALSMI 129 Query: 124 VTGTIWRWLLQPQGGVNVLPTLFGLPPLSFPWLATREQVL 163 VTGT W+WLL P G++ L +G F WL ++V+ Sbjct: 130 VTGTAWQWLLNPGLGLDKLLRDWGWEGFRFDWLVDPDRVI 169 Lambda K H 0.331 0.146 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: 335 Number of extensions: 14 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 369 Length of database: 305 Length adjustment: 28 Effective length of query: 341 Effective length of database: 277 Effective search space: 94457 Effective search space used: 94457 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.9 bits) S2: 49 (23.5 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
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:
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