Align Low-affinity putrescine importer PlaP (characterized)
to candidate 7026491 Shewana3_3634 amino acid permease-associated region (RefSeq)
Query= SwissProt::P0AA47 (452 letters) >FitnessBrowser__ANA3:7026491 Length = 443 Score = 575 bits (1482), Expect = e-168 Identities = 280/432 (64%), Positives = 342/432 (79%) Query: 14 LRKTLTLVPVVMMGLAYMQPMTLFDTFGIVSGLTDGHVPTAYAFALIAILFTALSYGKLV 73 L+++L+L VV+MGLAY+ PM +FDTFGIVS +T GHV T+Y AL ILFTA SYG LV Sbjct: 8 LKQSLSLWQVVVMGLAYLTPMAVFDTFGIVSEITSGHVATSYLLALAGILFTAFSYGHLV 67 Query: 74 RRYPSAGSAYTYAQKSISPTVGFMVGWSSLLDYLFAPMINILLAKIYFEALVPSIPSWMF 133 R+YP AGSAYTYAQK+ SP VGFMVGWSSLLDY+F PMIN+LLAKIY A+ P++ W+F Sbjct: 68 RKYPYAGSAYTYAQKTFSPNVGFMVGWSSLLDYMFMPMINMLLAKIYLTAMFPNVEPWIF 127 Query: 134 VVALVAFMTAFNLRSLKSVANFNTVIVVLQVVLIAVILGMVVYGVFEGEGAGTLASTRPF 193 + LVA MT NLR + VANFN VIV Q+ +I V +G++ + + GEG G +AS RPF Sbjct: 128 IFGLVAVMTVLNLRGIDLVANFNGVIVFAQIAIILVFIGLMAHSLSLGEGEGVIASVRPF 187 Query: 194 WSGDAHVIPMITGATILCFSFTGFDGISNLSEETKDAERVIPRAIFLTALIGGMIFIFAT 253 +S + + P+ TGATILCFSF GFDG+S+LSEETKDA+RVIPRAI LTALIGG+IF+ + Sbjct: 188 YSEEISLAPLFTGATILCFSFLGFDGLSSLSEETKDAKRVIPRAIVLTALIGGVIFVSVS 247 Query: 254 YFLQLYFPDISRFKDPDASQPEIMLYVAGKAFQVGALIFSTITVLASGMAAHAGVARLMY 313 YFLQL+FPDISRF+ DA PEI LYV G FQ L+ +TI VLASGMAAHAGVAR++Y Sbjct: 248 YFLQLFFPDISRFQQLDAVLPEIALYVGGNLFQSVVLVATTIAVLASGMAAHAGVARILY 307 Query: 314 VMGRDGVFPKSFFGYVHPKWRTPAMNIILVGAIALLAINFDLVMATALINFGALVAFTFV 373 VMGRD + P FGY+HPKWRTPA N+ILVG +AL A++FDL MA AL+NFGALVAFTFV Sbjct: 308 VMGRDNMLPNKGFGYIHPKWRTPAFNVILVGLLALSAVSFDLEMALALVNFGALVAFTFV 367 Query: 374 NLSVISQFWIREKRNKTLKDHFQYLFLPMCGALTVGALWVNLEESSMVLGLIWAAIGLIY 433 NLSVI QF+I+EKRN++LKDHFQY LP+CGA T+G LW+NLE S+ LGLIWAA+G++Y Sbjct: 368 NLSVIVQFYIKEKRNQSLKDHFQYFVLPLCGAATIGVLWINLEPQSLELGLIWAAVGILY 427 Query: 434 LACVTKSFRNPV 445 LA + R V Sbjct: 428 LALRSLRLRKAV 439 Lambda K H 0.328 0.140 0.424 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: 621 Number of extensions: 16 Number of successful extensions: 1 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: 452 Length of database: 443 Length adjustment: 33 Effective length of query: 419 Effective length of database: 410 Effective search space: 171790 Effective search space used: 171790 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 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