Align D-serine/L-alanine/D-alanine/glycine/D-cycloserine uptake porter of 556 aas, CycA (characterized)
to candidate WP_017177889.1 A1QA_RS0105330 amino acid permease
Query= TCDB::M1IW84 (556 letters) >NCBI__GCF_000295095.1:WP_017177889.1 Length = 479 Score = 541 bits (1395), Expect = e-158 Identities = 264/457 (57%), Positives = 339/457 (74%), Gaps = 5/457 (1%) Query: 16 HLRRDLANRHIQLIAIGGAIGTGLFMGSGRTISLAGPAVMVVYGIIGFFVFFVLRAMGEL 75 HL+R L NRHIQLIAIGGAIGTGLFMGSG+TISLAGP V++VY IIG F+F V+RA+GE+ Sbjct: 19 HLQRRLTNRHIQLIAIGGAIGTGLFMGSGKTISLAGPGVLLVYAIIGGFLFLVMRALGEV 78 Query: 76 LLSNLNYKSFVDFAADLLGPAAGFFVGWSYWFAWVVTGIADLVAITSYARFWWPGLPIWV 135 LLSNL YKSF D A DL+GP AGFF GW+Y+F W+VT IA+++AIT Y + WWP +P+W+ Sbjct: 79 LLSNLEYKSFADVAHDLIGPWAGFFTGWTYYFCWLVTAIAEVIAITQYVQHWWPTVPLWL 138 Query: 136 PALVTVALILAVNLFSVRHFGELEFWFALIKVAAIVCLIAVGAILVATNFVSPHGVHATI 195 PA VTVAL+L++NL +VR FGE+EFWF++IK+ AI+ L+ VG +LV F +P+G A++ Sbjct: 139 PATVTVALLLSLNLTTVRAFGEIEFWFSIIKIVAILALVVVGIVLVVIGFTAPNGAVASL 198 Query: 196 ENLWN----DNGFFPTGFLGVVSGFQIAFFAYIGVELVGTAAAETADPRRTLPRAINAVP 251 NL + FP GF G FQIA FA++G EL+GTAAAE DP TLP+AINA+P Sbjct: 199 GNLGDLSDPVGSLFPNGFSGFTGAFQIAVFAFVGTELIGTAAAEAKDPEVTLPKAINAIP 258 Query: 252 LRVAVFYIGALLAILAVVPWRQFASGESPFVTMFSLAGLAAAASVVNFVVVTAAASSANS 311 +R+ +FY+GAL AI+ V PWR+ + SPFV MFSLAG AAS+VNFVV+TAAASSANS Sbjct: 259 VRILLFYLGALTAIMMVTPWRE-VTESSPFVAMFSLAGFGLAASLVNFVVLTAAASSANS 317 Query: 312 GFFSTGRMLFGLADEGHAPAAFHQLNRGGVPAPALLLTAPLLLTSIPLLYAGRSVIGAFT 371 G +ST RML+GL+ H PA F +L VP PAL++T LLT+IPLLY S+I AFT Sbjct: 318 GMYSTSRMLYGLSWSEHGPAVFKRLTSRSVPGPALVVTCAALLTAIPLLYTTSSIIDAFT 377 Query: 372 LVTTVSSLLFMFVWAMIIISYLVYRRRHPQRHTDSVYKMPGGVVMCWAVLVFFAFVIWTL 431 +VTTV+S+LF+ VW +I++SYL +R HP+RH S +KMPG V WA +VFFAFV+WTL Sbjct: 378 VVTTVASVLFILVWIIIVVSYLRFRSLHPERHEASAFKMPGDRVSAWASIVFFAFVVWTL 437 Query: 432 TTETETATALAWFPLWFVLLAVGWLVTQRRQSRRSFG 468 +T A+ PLW V++A W + +RR G Sbjct: 438 IQAEDTRLAVLVSPLWLVVMASAWWWLRSGAARRLAG 474 Lambda K H 0.328 0.140 0.442 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: 716 Number of extensions: 31 Number of successful extensions: 3 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: 556 Length of database: 479 Length adjustment: 35 Effective length of query: 521 Effective length of database: 444 Effective search space: 231324 Effective search space used: 231324 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: 52 (24.6 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