Align N-acetylglucosamine transporter nagP (characterized)
to candidate 5208608 Shew_1119 glucose/galactose transporter (RefSeq)
Query= reanno::ANA3:7025962 (432 letters) >FitnessBrowser__PV4:5208608 Length = 418 Score = 728 bits (1878), Expect = 0.0 Identities = 370/418 (88%), Positives = 388/418 (92%), Gaps = 1/418 (0%) Query: 15 MAIVAALFFILGFATWLNGSLMPYLKQILQLNPFQASLILFSFYIAVTFTALPSAWVIRK 74 MAIVA LFFILGFATWLNGSLMPYLKQILQL P QASLILFSFYIAVTFTALPSAWVIRK Sbjct: 1 MAIVAGLFFILGFATWLNGSLMPYLKQILQLTPLQASLILFSFYIAVTFTALPSAWVIRK 60 Query: 75 VGYKNGMALGMGIMMLAGLLFIPAAKTQIFGLFLCAQLVMGTGQTLLQTAVNPYVVRLGP 134 VGYK GMA+GMGIMM+AGLLFIPAAKTQ+F LFL AQLVMGTGQTLLQTAVNPYVVR+GP Sbjct: 61 VGYKTGMAMGMGIMMIAGLLFIPAAKTQVFALFLFAQLVMGTGQTLLQTAVNPYVVRIGP 120 Query: 135 EESAAARVSVMGILNKGAGVIAPLVFSALILDSFKDRIGTTLTQVQIDEMANSLVFPYLG 194 EESAAARVSVMGILNKGAGVIAPLVF+ALILDSFKDR+G LTQ QIDEMAN LVFPYLG Sbjct: 121 EESAAARVSVMGILNKGAGVIAPLVFTALILDSFKDRVGVELTQAQIDEMANGLVFPYLG 180 Query: 195 MAIFIGVLALAVKKSPLPELSNEDEVAEHTDKGQIKAALSHPNLAFGVIALFVYVAVEVI 254 MAIFIGVLAL VKKSPLPEL NEDE E T KG + ALSHPNLA GV+ALF YVAVEVI Sbjct: 181 MAIFIGVLALLVKKSPLPELENEDEQEEGT-KGHTREALSHPNLALGVVALFFYVAVEVI 239 Query: 255 AGDTIGTFALSLGVEHYGVMTSYTMVCMVLGYTLGIILIPRFISQPTALMISAILGLLLT 314 AGDTIGTFALSLGVE+YGVMTSYTM+CMV+GY+LGI+ IPRFISQP ALMISAILGL+LT Sbjct: 240 AGDTIGTFALSLGVENYGVMTSYTMICMVIGYSLGILTIPRFISQPKALMISAILGLMLT 299 Query: 315 LAILFGDNNSYAIANALLVPFGGVALPDTLLFIAFLGLANAIVWPAVWPLALSGLGKLTS 374 L ILFGDN SYAIANALLVPFGG LPDTLL IAFLGLANAIVWPAVWPLALSG+GKLTS Sbjct: 300 LGILFGDNESYAIANALLVPFGGAMLPDTLLMIAFLGLANAIVWPAVWPLALSGMGKLTS 359 Query: 375 TGSALLIMGIAGGAFGPLFWGLTSSATDMGQQGGYMVMLPCYLFILFYAVKGHKMRHW 432 TGSALL+MGIAGGAFGPLFWGLTSSAT +GQQGGYMVMLPCYLFILFYAVKG+KMR W Sbjct: 360 TGSALLVMGIAGGAFGPLFWGLTSSATSLGQQGGYMVMLPCYLFILFYAVKGYKMRSW 417 Lambda K H 0.327 0.141 0.421 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: 839 Number of extensions: 38 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: 432 Length of database: 418 Length adjustment: 32 Effective length of query: 400 Effective length of database: 386 Effective search space: 154400 Effective search space used: 154400 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 (21.7 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