Align Serine uptake transporter, SerP1, of 259 aas and 12 TMSs (Trip et al. 2013). L-serine is the highest affinity substrate (Km = 18 μM), but SerP1 also transports L-threonine and L-cysteine (Km values = 20 - 40 μM) (characterized)
to candidate WP_084933921.1 HA51_RS07520 aromatic amino acid transporter AroP
Query= TCDB::F2HQ25 (459 letters) >NCBI__GCF_002095475.1:WP_084933921.1 Length = 451 Score = 281 bits (718), Expect = 4e-80 Identities = 158/447 (35%), Positives = 247/447 (55%), Gaps = 22/447 (4%) Query: 5 QEKHEAQRGLQNRHIQLIAIAGTIGTGLFLGAGKTIQMTGPSVIFAYILIGIAMFFFLRT 64 Q RGL+NRHIQLIA+ G +GTGLFLG+ I+ GP+VI Y + G F +R Sbjct: 4 QHGESLHRGLKNRHIQLIALGGAVGTGLFLGSASVIKSAGPAVILGYAIAGFIAFLIMRQ 63 Query: 65 IGEMLYNDPSQHSFLNFVTKYSGVRTGYFTQWSYWLVIVFVCISELTAIGTYIQFWLPQV 124 +GEM+ +P SF +F KY G G+ + W+YW++ V V ++EL+A+G YIQFW P+ Sbjct: 64 LGEMVVEEPVAGSFSHFAYKYWGNFAGFASGWNYWVLYVLVAMAELSAVGKYIQFWYPEF 123 Query: 125 PLWLIEIVMLALLFGLNTLNSRFFGETEFWFAMIKVAAIIGMIV-TAIILVAGNFHYSTV 183 P W + ++ +N N + FGE EFWFA+IKV A+IGMI+ +L +GN Sbjct: 124 PTWASAAIFFVVINAINLTNVKVFGEMEFWFAIIKVVAVIGMILFGGWLLFSGN------ 177 Query: 184 LSGKTVHDSASLSNIFDGFQLFPHGAWNFVGALQMVMFAFTSMEFIGMTAAETVNPKKSL 243 AS++N++ PHG V + ++MF+F +E +G+TAAE NP++S+ Sbjct: 178 -----AGPQASVTNLWSQGGFLPHGMTGLVMMMAIIMFSFGGLELVGITAAEADNPQESI 232 Query: 244 PKAINQIPVRILLFYVGALLAIMAIFNWHYIPADKSPFVMVFQLIGIKWAAALINFVVLT 303 PKA NQ+ RIL+FY+G+L ++++ W + + SPFV++F +G + A +N V+LT Sbjct: 233 PKATNQVLWRILIFYIGSLTVLLSLMPWTRVTEETSPFVLIFHELGDAFVANALNVVILT 292 Query: 304 SAASALNSSLFSATRNMYSLAQQHDKGRLTPFTKLSKAGIPI-NALYMATALSLLAPVLT 362 +A S NS ++ +R ++ LAQQ + + + K G+P+ L A A +L + Sbjct: 293 AALSVYNSCVYCNSRMLFGLAQQGNAPK--ALLNVDKRGVPVATILVSAVATALCVLINY 350 Query: 363 LIPQIKNAFDFAASCTTNLFLVVYFITLYTYWQYRKSEDYNPKGFLTPKPQITVPF-IVA 421 L+P AF S + ++ + + + ++RK +D +G T + PF Sbjct: 351 LMP--GEAFGLLMSLVVSALVINWAMISLAHMKFRKKKD--QQGVTTRFRAVLYPFGNWL 406 Query: 422 IFAIVFASLFFNADTFYPALGAIVWTI 448 A + A L A T P + VW I Sbjct: 407 CLAFMAAVLVIMAIT--PGMAISVWLI 431 Lambda K H 0.329 0.141 0.434 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: 593 Number of extensions: 31 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: 459 Length of database: 451 Length adjustment: 33 Effective length of query: 426 Effective length of database: 418 Effective search space: 178068 Effective search space used: 178068 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: 51 (24.3 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