Align N-acetylglucosamine porter, NagP (characterized)
to candidate 7025545 Shewana3_2696 major facilitator transporter (RefSeq)
Query= TCDB::Q8EBL0 (435 letters) >FitnessBrowser__ANA3:7025545 Length = 452 Score = 416 bits (1069), Expect = e-121 Identities = 226/431 (52%), Positives = 296/431 (68%), Gaps = 16/431 (3%) Query: 9 KSSFLPMAIVAALFFILGFATWLNGSLMPYLKQILQLNPFQASLILFSFYIAVTFTALPS 68 + SF+PM ++ LFF+ GF TWLNG+L+P+LK QLN F+A L+ F FYIA ALP+ Sbjct: 15 QGSFIPMLLIGILFFVFGFVTWLNGALIPFLKIACQLNEFEAYLVTFVFYIAYFVMALPT 74 Query: 69 AWVIRKVGYKNGMALGMGVMMIAGLLFIPAAKTQVFALFLFAQLVMGAGQTLLQTAVNPY 128 + ++ ++GYK GM LG+G+M LFI AA FA FL A V+G G TLLQTA NPY Sbjct: 75 SSILTRLGYKMGMTLGLGIMAAGAGLFIVAALVGHFATFLLALFVLGTGLTLLQTAANPY 134 Query: 129 VVRLGPEESAAARVSVMGILNKGAGVIAPLVFSALILDSFKDRIGTTLT-------QVQI 181 +V +GP ESAA R+S+MGI+NKGAG I P++F+A IL + T L Q+ + Sbjct: 135 IVCIGPRESAAMRISLMGIVNKGAGFIVPIIFTAWILTGMEPYSETALASLSEAQRQLAL 194 Query: 182 DEMANGLVLPYLGMA-VFIGILALAVKKSPLPELSNEDEVADHTDKSQI--KAALSHPNL 238 E+AN LV PYL M V +G++A V SPLPE E+ + +++Q KA L +P + Sbjct: 195 TELANRLVHPYLMMMLVLLGLMAF-VWFSPLPE----PELGERVERTQTDWKAILQYPQV 249 Query: 239 ALGVLALFVYVAVEVIAGDTIGTFALSLGIDHYGVMTSYTMVCMVLGYILGILLIPRVIS 298 LG L LF YV EVIAGD+IG F+ LG+ H+G+MTSYTM MVLGY+LGILLIPR IS Sbjct: 250 ILGALTLFCYVGAEVIAGDSIGLFSQGLGVAHFGMMTSYTMGFMVLGYVLGILLIPRWIS 309 Query: 299 QPTALMISAILGLLLTLGILFGDNNSYAIANLLLVPFGGVALPDTLLLIAFLGLANAIVW 358 Q TAL+ SAI GLL TLG+L D+ S A++ LLL G + +PD +L +A LGLANA+VW Sbjct: 310 QQTALVGSAIAGLLFTLGVLLSDSQSQALSELLLGWLGVLPVPDPVLYLALLGLANALVW 369 Query: 359 PAVWPLALSGMGKLTSTGSALLIMGIAGGAFGPVSWGLMSSATDMGQQGGYMVMLPCYLF 418 PAVWPLAL G+G+LT+T SALLIMGIAGGA P+ +G ++ + Q Y ++LPCY Sbjct: 370 PAVWPLALEGLGRLTATASALLIMGIAGGAILPLLYGYIAHSQGDSQM-AYFLLLPCYGL 428 Query: 419 ILFYAVKGHKM 429 I +YA+ GHK+ Sbjct: 429 IFYYAIWGHKL 439 Lambda K H 0.326 0.141 0.414 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: 771 Number of extensions: 35 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: 435 Length of database: 452 Length adjustment: 32 Effective length of query: 403 Effective length of database: 420 Effective search space: 169260 Effective search space used: 169260 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 51 (24.3 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 paper from 2022 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