Chaperone/Protein Folding, cyclophilin 15 CYP15
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HYT6
Term | Name | Level | Count |
---|---|---|---|
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0018193 | peptidyl-amino acid modification | 5 | 12 |
GO:0018208 | peptidyl-proline modification | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016859 | cis-trans isomerase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.508 |
CLV_PCSK_FUR_1 | 284 | 288 | PF00082 | 0.736 |
CLV_PCSK_FUR_1 | 457 | 461 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.790 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.595 |
DEG_SPOP_SBC_1 | 421 | 425 | PF00917 | 0.695 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.592 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.488 |
DOC_CKS1_1 | 92 | 97 | PF01111 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 73 | 79 | PF00134 | 0.540 |
DOC_MAPK_FxFP_2 | 37 | 40 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 58 | 67 | PF00069 | 0.401 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.572 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.526 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.381 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.427 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.572 |
DOC_USP7_MATH_2 | 76 | 82 | PF00917 | 0.475 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.771 |
DOC_USP7_UBL2_3 | 455 | 459 | PF12436 | 0.671 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 139 | 143 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 149 | 154 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 214 | 223 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 362 | 368 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 418 | 427 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 58 | 67 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 198 | 215 | PF00022 | 0.542 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.641 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.631 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 444 | 448 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_2 | 319 | 325 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_2 | 326 | 332 | PF00533 | 0.657 |
LIG_BRCT_BRCA1_2 | 444 | 450 | PF00533 | 0.595 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.380 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.456 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.621 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.567 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.535 |
LIG_LIR_Apic_2 | 34 | 40 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 242 | 251 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 379 | 386 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.488 |
LIG_MLH1_MIPbox_1 | 320 | 324 | PF16413 | 0.629 |
LIG_REV1ctd_RIR_1 | 321 | 329 | PF16727 | 0.681 |
LIG_REV1ctd_RIR_1 | 381 | 389 | PF16727 | 0.626 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 92 | 96 | PF00017 | 0.536 |
LIG_SH2_PTP2 | 181 | 184 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.556 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.518 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.412 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.551 |
LIG_TYR_ITIM | 165 | 170 | PF00017 | 0.514 |
LIG_TYR_ITIM | 241 | 246 | PF00017 | 0.614 |
LIG_WRC_WIRS_1 | 246 | 251 | PF05994 | 0.453 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.400 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.425 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.696 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.739 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.680 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.500 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.504 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.532 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.579 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.504 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.426 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.604 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.434 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.724 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.643 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.606 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.601 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.739 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.705 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.739 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.505 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.373 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.389 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.592 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.569 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.609 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.683 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.643 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.667 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.409 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.379 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.449 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.576 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.483 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.605 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.545 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.611 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.762 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.401 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.513 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.516 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.585 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.761 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.466 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.568 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.766 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.608 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.489 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.542 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.480 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.515 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.454 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.333 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.417 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.478 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.497 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.563 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.561 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.542 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.521 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 207 | 215 | PF00179 | 0.539 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.629 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.730 |
TRG_NLS_Bipartite_1 | 213 | 233 | PF00514 | 0.588 |
TRG_NLS_MonoCore_2 | 343 | 348 | PF00514 | 0.661 |
TRG_NLS_MonoExtC_3 | 343 | 349 | PF00514 | 0.600 |
TRG_NLS_MonoExtC_3 | 453 | 458 | PF00514 | 0.742 |
TRG_NLS_MonoExtN_4 | 228 | 233 | PF00514 | 0.575 |
TRG_NLS_MonoExtN_4 | 341 | 348 | PF00514 | 0.639 |
TRG_NLS_MonoExtN_4 | 453 | 458 | PF00514 | 0.666 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC45 | Leptomonas seymouri | 57% | 100% |
A0A0S4KRJ3 | Bodo saltans | 31% | 100% |
A0A1X0NWC9 | Trypanosomatidae | 34% | 100% |
A0A3S7WVY2 | Leishmania donovani | 99% | 100% |
A0A422NPI7 | Trypanosoma rangeli | 36% | 100% |
C9ZIB2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AIE5 | Leishmania braziliensis | 76% | 100% |
E9AUN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4QCV2 | Leishmania major | 88% | 100% |
V5DRZ7 | Trypanosoma cruzi | 38% | 100% |