Align δ1-pyrroline-5-carboxylate synthetase (EC 1.2.1.41; EC 2.7.2.11) (characterized)
to candidate Pf1N1B4_2688 Gamma-glutamyl phosphate reductase (EC 1.2.1.41)
Query= metacyc::AT2G39800-MONOMER (717 letters) >lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_2688 Gamma-glutamyl phosphate reductase (EC 1.2.1.41) Length = 415 Score = 272 bits (695), Expect = 3e-77 Identities = 150/404 (37%), Positives = 241/404 (59%), Gaps = 6/404 (1%) Query: 301 AARESSRKLQALSSEDRKKILLDIADALEANVTTIKAENELDVASAQEAGLEESMVARLV 360 AARE+SR + S+ + + L A+AL+A + A NELD+A+ + GLE +++ RL Sbjct: 7 AAREASRVIGRASTAQKNRALQAAANALDAARAELTAANELDLAAGRANGLEPALLERLA 66 Query: 361 MTPGKISSLAASVRKLADMEDPIGRVLKKTEVADGLVLEKTSSPLGVLLIVFESRPDALV 420 +TP +I + +R++A + DP+G + + G+ + K PLGV+ I++ESRP+ + Sbjct: 67 LTPERIDGMIVGLRQVAALPDPVGAIRDMSYRPSGIQVGKMRVPLGVIGIIYESRPNVTI 126 Query: 421 QIASLAIRSGNGLLLKGGKEARRSNAILHKVITDAIPET-VGGKLIGLV--TSREEIPDL 477 ASL ++SGN +L+GG EA SN + I + E + ++ +V T R + L Sbjct: 127 DAASLCLKSGNATILRGGSEAIHSNRAIAACIQRGLAEAGLPAAVVQVVETTDRAAVGAL 186 Query: 478 LKLDDVIDLVIPRGSNKLVTQIKNTTKIPVLGHADGICHVYVDKACDTDMAKRIVSDAKL 537 + + + +D+++PRG L+ ++ ++PV+ H DGICHVYV D A+RI +AK Sbjct: 187 ITMPEYVDVIVPRGGRGLIERVSRDARVPVIKHLDGICHVYVSAHADLPKAQRIAFNAKT 246 Query: 538 DYPAACNAMETLLVHKDLEQNAVLNELIFALQSNGVTLYGGPRASKILNIPEA--RSFNH 595 C AMETLLV + + ++ L + L+ GV L G R I+ A ++ Sbjct: 247 YRYGICGAMETLLVDQAVAKD-FLPSMAAQLREKGVELRGCERTRAIIEAVAATEEDWHT 305 Query: 596 EYCAKACTVEVVEDVYGAIDHIHRHGSAHTDCIVTEDHEVAELFLRQVDSAAVFHNASTR 655 EY A ++ VV+ + AI+HI+++GS HTD IV+E+ F+ +VDS++V N T Sbjct: 306 EYLAPILSIRVVDGLDQAIEHINKYGSHHTDSIVSENLADTRRFVAEVDSSSVMINTPTC 365 Query: 656 FSDGFRFGLGAEVGVSTGRIHARGPVGVEGLLTTRWIMRGKGQV 699 F+DGF +GLGAE+G+ST ++HARGPVG+EGL ++I+ G GQ+ Sbjct: 366 FADGFEYGLGAEIGISTDKLHARGPVGLEGLTCEKYIVVGDGQL 409 Lambda K H 0.318 0.135 0.378 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: 600 Number of extensions: 22 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: 717 Length of database: 415 Length adjustment: 35 Effective length of query: 682 Effective length of database: 380 Effective search space: 259160 Effective search space used: 259160 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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, or see changes to Amino acid biosynthesis since the publication.
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