Align 1-pyrroline-5-carboxylate dehydrogenase 2; P5C dehydrogenase 2; L-glutamate gamma-semialdehyde dehydrogenase; EC 1.2.1.88 (characterized)
to candidate WP_068173812.1 HTA01S_RS16360 aldehyde dehydrogenase family protein
Query= SwissProt::P94391 (515 letters) >NCBI__GCF_001592305.1:WP_068173812.1 Length = 483 Score = 260 bits (665), Expect = 7e-74 Identities = 163/466 (34%), Positives = 237/466 (50%), Gaps = 21/466 (4%) Query: 53 VSINPADKEEVVGRVSKASQEHAEQAIQAAAKAFEEWRYTSPEERAAVLFRAAAKVRRRK 112 VS NP+D EVV ++A + E AI+AAA A W +SP+ RA VL + +++ RK Sbjct: 26 VSTNPSDTREVVAEYARADRNQTELAIRAAADALPHWSQSSPQRRADVLDQIGSELLARK 85 Query: 113 HEFSALLVKEAGKPWNEADADTAEAIDFMEYYARQMIELAKGKPVNSREGEKNQYVYTPT 172 E ALL +E GK E + A A +++A + + + + R G + P Sbjct: 86 DELGALLAREEGKTLPEGVGEVARAGQIFKFFAGEALRIPGEVIASVRPGVRVDVTREPV 145 Query: 173 GVTVVIPPWNFLFAIMAGTTVAPIVTGNTVVLKPASATPVIAAKFVEVLEESGLPKGVVN 232 GV +I PWNF FAI A + GNTVV KPA P E++ GLP GV N Sbjct: 146 GVVGIIAPWNFPFAIPAWKIAPALAYGNTVVFKPAELVPACGWALAEIISRCGLPAGVFN 205 Query: 233 FVPGSGAEVGDYLVDHPKTSLITFTGSREVGTRIFE----RAAKVQPGQQHLKRVIAEMG 288 V GSG EVG LVDHP + ++FTGS G RI + R AKVQ EMG Sbjct: 206 LVMGSGREVGQTLVDHPLVNALSFTGSVSTGERILKAATARRAKVQ----------LEMG 255 Query: 289 GKDTVVVDEDADIELAAQSIFTSAFGFAGQKCSAGSRAVVHEKVYDQVLERVIEITESKV 348 GK+ +VV DAD++ A ++ GQ+C+A SR +V +V+D + ++ + + Sbjct: 256 GKNPLVVLADADLDQAVDCALQGSYFSTGQRCTASSRLIVQAQVHDAFVAKLRQRLSTLK 315 Query: 349 TAKPDSADVYMGPVIDQGSYDKIMSYIEIGKQEG-RLVSGG--TGDDSKGYFIKPTIFAD 405 MGPV+D+ ++ ++YIEI + EG V GG + G+++ P +F Sbjct: 316 VGHALERGTEMGPVVDRAQLEQNLAYIEIARNEGAEHVWGGDLLQRPTPGHYMSPALFL- 374 Query: 406 LDPKARLMQEEIFGPVVAFCKVSDFDEALEVANNTEYGLTGAVITNNRKHIERAKQEFHV 465 P+ R+ +EEIFGPV + D++ AL +AN+T +GL + T + K+ K+ V Sbjct: 375 AKPEHRVAREEIFGPVACVLRADDYEHALVLANDTPFGLCAGICTTSLKYAMHFKRHAEV 434 Query: 466 GNLYFNRNCTGAIVGYH-PFGGFKMSGTDSKAGGPDYLALHMQAKT 510 G N G V +H PFGG K S S+ G + + KT Sbjct: 435 GMTMVNLPTAG--VDFHVPFGGRKESSHGSREQGRYAVEFYTTVKT 478 Lambda K H 0.316 0.133 0.379 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: 561 Number of extensions: 32 Number of successful extensions: 4 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: 515 Length of database: 483 Length adjustment: 34 Effective length of query: 481 Effective length of database: 449 Effective search space: 215969 Effective search space used: 215969 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 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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