Align Serine transporter (characterized)
to candidate WP_112255899.1 AS188_RS01560 HAAAP family serine/threonine permease
Query= SwissProt::P0AAD6 (429 letters) >NCBI__GCF_001482365.1:WP_112255899.1 Length = 403 Score = 387 bits (993), Expect = e-112 Identities = 193/406 (47%), Positives = 273/406 (67%), Gaps = 6/406 (1%) Query: 22 DTMWMLGLYGTAIGAGVLFLPINAGVGGMIPLIIMAILAFPMTFFAHRGLTRFVLSGKNP 81 DT W + L+GTA+GAG+LFLPINAG GG+ PL+++ L PMT+ +HR L RFV + Sbjct: 2 DTAWTISLFGTAVGAGILFLPINAGAGGLWPLLVVTALIGPMTYLSHRALARFVCASPRR 61 Query: 82 GEDITEVVEEHFGIGAGKLITLLYFFAIYPILLVYSVAITNTVESFMSHQLGMTPPPRAI 141 GEDIT V ++FG GAG++IT+LYF AIYPI+L+Y V ITNTV+S + +QLG+ P PR + Sbjct: 62 GEDITAVARDYFGDGAGRVITVLYFLAIYPIVLIYGVGITNTVDSLLVNQLGLPPVPRVL 121 Query: 142 LSLILIVGMMTIVRFGEQMIVKAMSILVFPFVGVLMLLALYLIPQWNGAALETLSLDTAS 201 LS +LI MM ++ G+++++ LV+P + L+ + LYL+P W+ L A Sbjct: 122 LSGVLIAAMMVVMVAGQRIMLAVTQWLVYPLILALLGVTLYLVPSWHVGDL------AAV 175 Query: 202 ATGNGLWMTLWLAIPVMVFSFNHSPIISSFAVAKREEYGDMAEQKCSKILAFAHIMMVLT 261 + L ++WL IPV+VF+FNHSP IS F++A + +G A + S++L ++V+ Sbjct: 176 PSAGDLAASVWLVIPVLVFAFNHSPAISQFSLAMQRAHGAGAAEAASRVLRRTTALLVVF 235 Query: 262 VMFFVFSCVLSLTPADLAAAKEQNISILSYLANHFNAPVIAWMAPIIAIIAITKSFLGHY 321 M FV+SCVL+L LA A+E N+ +LS+LAN P+I ++ P +AI AI SF GHY Sbjct: 236 TMGFVWSCVLALGADGLAGAREANLPVLSHLANELGNPLIGYLGPAVAIAAIVSSFFGHY 295 Query: 322 LGAREGFNGMVIKSLRGKGKSIEINKLNRITALFMLVTTWIVATLNPSILGMIETLGGPI 381 LGA EG G+V L + L A+F+ +TTW+ A LNPSILG+IE+L GP+ Sbjct: 296 LGASEGAAGIVRGLLPARVPQPRERTLRGGIAVFVFLTTWLAAVLNPSILGLIESLAGPV 355 Query: 382 IAMILFLMPMYAIQKVPAMRKYSGHISNVFVVVMGLIAISAIFYSL 427 IA IL+LMPMYAI+++PA+ Y G +SNVFV V G++AIS I +SL Sbjct: 356 IAAILYLMPMYAIRRIPALAPYRGRLSNVFVTVAGIVAISGILFSL 401 Lambda K H 0.328 0.140 0.416 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: 567 Number of extensions: 29 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: 429 Length of database: 403 Length adjustment: 31 Effective length of query: 398 Effective length of database: 372 Effective search space: 148056 Effective search space used: 148056 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 (21.8 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 24 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:
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