Align D-serine/D-alanine/glycine transporter (characterized)
to candidate Pf6N2E2_5633 Aromatic amino acid transport protein AroP
Query= SwissProt::P0AAE0 (470 letters) >FitnessBrowser__pseudo6_N2E2:Pf6N2E2_5633 Length = 472 Score = 350 bits (897), Expect = e-101 Identities = 178/458 (38%), Positives = 284/458 (62%), Gaps = 17/458 (3%) Query: 19 LRRNLTNRHIQLIAIGGAIGTGLFMGSGKTISLAGPSIIFVYMIIGFMLFFVMRAMGELL 78 L+R L NRHIQLIA+GGAIGTGLF+GS + AGPS+I Y I GF+ F +MR +GE++ Sbjct: 11 LKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPSMILGYAICGFIAFMIMRQLGEMI 70 Query: 79 LSNLEYKSFSDFASDLLGPWAGYFTGWTYWFCWVVTGMADVVAITAYAQFWFPDLSDWVA 138 + SFS FA G +AG+ +GW W +++ GM+++ A+ Y +W PD+ WV+ Sbjct: 71 VEEPVAGSFSHFAHKYWGGFAGFLSGWNCWILYILVGMSELTAVGKYIHYWAPDIPTWVS 130 Query: 139 SLAVIVLLLTLNLATVKMFGEMEFWFAMIKIVAIVSLIVVG-LVMVAMHFQSPTGVEASF 197 + A +L+ +NLA VK+FGE EFWFA+IK+VAIV +I +G ++V+ H G +AS Sbjct: 131 AAAFFILINVINLANVKVFGEAEFWFAIIKVVAIVGMIALGSYLLVSGH----GGPQASV 186 Query: 198 AHLWNDGGWFPKGLSGFFAGFQIAVFAFVGIELVGTTAAETKDPEKSLPRAINSIPIRII 257 +LW+ GG+FP G+SG I +F+F G+E++G TAAE P+ +P+AIN + RI+ Sbjct: 187 TNLWSHGGFFPNGVSGLVMAMAIIMFSFGGLEMLGFTAAEADKPKTVIPKAINQVIYRIL 246 Query: 258 MFYVFALIVIMSVTPWSSVVP---------EKSPFVELFVLVGLPAAASVINFVVLTSAA 308 +FY+ AL+V++S+TPW S++ SPFV++F ++G AA ++NFVVLT+A Sbjct: 247 IFYIGALVVLLSLTPWDSLLSTLNASGDAYSGSPFVQVFSMLGSNTAAHILNFVVLTAAL 306 Query: 309 SSANSGVFSTSRMLFGLAQEGVAPKAFAKLSKRAVPAKGLTFSCICLLGGVVMLYVNPSV 368 S NSG + SRML G+A++G APK +K+ KR VP + + S L V++ Y+ P Sbjct: 307 SVYNSGTYCNSRMLLGMAEQGDAPKVLSKIDKRGVPVRSILASAAVTLVAVLLNYLIPQ- 365 Query: 369 IGAFTMITTVSAILFMFVWTIILCSYLVYRKQRPHLHEKSIYKMPLGKLMCWVCMAFFVF 428 A ++ ++ + W +I S+ +R+ H+ ++K ++C+AF VF Sbjct: 366 -HALELLMSLVVATLVINWAMISYSHFKFRQHMNQTHQTPLFKALWYPYGNYICLAFVVF 424 Query: 429 VVVLLTLEDDTRQALLVTPLWFIALGLGWLFIGKKRAA 466 ++ ++ L + ++ P+W + + + + +I KR+A Sbjct: 425 ILGVMLLIPGIQVSVYAIPVWVVFMAVCY-WIKNKRSA 461 Lambda K H 0.329 0.141 0.440 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: 583 Number of extensions: 30 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 470 Length of database: 472 Length adjustment: 33 Effective length of query: 437 Effective length of database: 439 Effective search space: 191843 Effective search space used: 191843 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 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:
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