Align ABC transporter for D-Glucose-6-Phosphate, periplasmic substrate-binding component (characterized)
to candidate GFF1918 PGA1_c19500 putative sugar-binding periplasmic protein
Query= reanno::WCS417:GFF4324 (428 letters) >lcl|FitnessBrowser__Phaeo:GFF1918 PGA1_c19500 putative sugar-binding periplasmic protein Length = 414 Score = 206 bits (523), Expect = 1e-57 Identities = 144/420 (34%), Positives = 196/420 (46%), Gaps = 22/420 (5%) Query: 13 IASLFPLSAFAADSKGTVEVVHWWTSGGEKAAVDVLKAQVEKDGFVWKDGAVAGGGGATA 72 +A+L SA AD EV+HWW S GE AA+ V +G W D + GGG A Sbjct: 11 VATLAMTSAATADGI-RAEVIHWWVSAGEAAAIKVFADAYTANGGEWIDNGIGGGG---A 66 Query: 73 MTVLKSRAVAGNPPGVAQIK-GPDIQEWASTGLLDTDVLKDVAKEEKWDSLLDKKVSDTV 131 T +R + G+ P V Q + +E GLL + L A+ W +L + + V Sbjct: 67 KTTFVNRLMGGDAPQVGQFNTSREFEEIVDAGLLHS--LDAEAEAGNWSALFPGIIDNVV 124 Query: 132 KYEGDYVAVPVNIHRVNWLWINPEVFKKAGITKNPTTLQEFYAAGDKLKAAGFIPLAHGG 191 K +G Y AVPVNIH NWLW N +V AG+ PT F+ A + LK AG IPLA GG Sbjct: 125 KRDGSYYAVPVNIHGSNWLWHNNQVMADAGLDV-PTDWDSFFEAAETLKEAGIIPLAVGG 183 Query: 192 QPWQDSTVFEAVVLSVMGADGYKKALVDLDNGALTGPEMVKALTELKKVATYM---DVDG 248 + WQ+ F +V+LSV G D Y + + D ALT EM + ++ T + D Sbjct: 184 EAWQERLTFNSVLLSVGGQDLYLRLFEEKDTTALTSDEMKEVFDVYSRLRTLVRETDPGS 243 Query: 249 KGQDWNLEAGKVINGKAGMQIMGDWAKSEWTAAKKVAGKDYECVAFPGTDKAFTYNIDSL 308 G+ WN VI G+A MQIMGDWAK E+ +A G +Y C + + D Sbjct: 244 PGRSWNDATNMVITGQAAMQIMGDWAKGEFLSAGMTPGVEYGCTPAVIAGSPYMISGDVF 303 Query: 309 AVFKQKDKGTAAGQQDIAKVVLGENFQKVFSINKGSIPVRNDMLNKMDSYGFDSCAQTA- 367 K ++ Q +A +L Q F+ KGSIPVR D +D+ D C Q A Sbjct: 304 VFPKTGNEEDREAQSLMATTMLDAEVQVAFNNIKGSIPVRPD----VDTSQLDVCGQQAI 359 Query: 368 AKDFLADAKTGGLQPSMAHNMATTLAVQGAFFDVVTNYINDPKADPADTAKKLGAAIKSA 427 A D G Q ++ ++A GA DV T + N + L A + A Sbjct: 360 ALTSNPDTHVGVTQMYISSDLA------GALQDVYTQFWNSETMTTEEAITLLSQAYEIA 413 Lambda K H 0.314 0.131 0.388 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: 488 Number of extensions: 20 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: 428 Length of database: 414 Length adjustment: 32 Effective length of query: 396 Effective length of database: 382 Effective search space: 151272 Effective search space used: 151272 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (22.0 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
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