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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9B4C7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.411 |
CLV_Separin_Metazoa | 382 | 386 | PF03568 | 0.629 |
DOC_CYCLIN_RxL_1 | 334 | 344 | PF00134 | 0.642 |
DOC_CYCLIN_RxL_1 | 447 | 461 | PF00134 | 0.602 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.649 |
DOC_MAPK_DCC_7 | 25 | 33 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 216 | 227 | PF00069 | 0.669 |
DOC_MAPK_gen_1 | 25 | 33 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 447 | 456 | PF00069 | 0.567 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.641 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.625 |
DOC_PP2B_PxIxI_1 | 89 | 95 | PF00149 | 0.485 |
DOC_PP4_FxxP_1 | 234 | 237 | PF00568 | 0.586 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.462 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 130 | 134 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 220 | 225 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 337 | 347 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 385 | 390 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 75 | 80 | PF00244 | 0.563 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 398 | 406 | PF00928 | 0.543 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.411 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.637 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.636 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.799 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.762 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.700 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.608 |
LIG_GBD_Chelix_1 | 103 | 111 | PF00786 | 0.411 |
LIG_Integrin_isoDGR_2 | 214 | 216 | PF01839 | 0.470 |
LIG_Integrin_isoDGR_2 | 73 | 75 | PF01839 | 0.595 |
LIG_LIR_Apic_2 | 231 | 237 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 459 | 463 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 175 | 182 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 404 | 412 | PF02991 | 0.728 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 194 | 198 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.632 |
LIG_NRBOX | 102 | 108 | PF00104 | 0.378 |
LIG_NRBOX | 188 | 194 | PF00104 | 0.651 |
LIG_PCNA_yPIPBox_3 | 473 | 481 | PF02747 | 0.552 |
LIG_PDZ_Class_1 | 481 | 486 | PF00595 | 0.612 |
LIG_Pex14_1 | 401 | 405 | PF04695 | 0.576 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.513 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.676 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.556 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.648 |
LIG_SH2_GRB2like | 148 | 151 | PF00017 | 0.589 |
LIG_SH2_GRB2like | 230 | 233 | PF00017 | 0.558 |
LIG_SH2_GRB2like | 460 | 463 | PF00017 | 0.689 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.771 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.588 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.590 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.465 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.611 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.730 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.746 |
LIG_SUMO_SIM_anti_2 | 108 | 115 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 452 | 459 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 108 | 115 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 452 | 459 | PF11976 | 0.584 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.588 |
LIG_TYR_ITIM | 389 | 394 | PF00017 | 0.576 |
LIG_WRC_WIRS_1 | 113 | 118 | PF05994 | 0.513 |
MOD_CDK_SPxK_1 | 349 | 355 | PF00069 | 0.692 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.473 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.536 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.436 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.574 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.793 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.629 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.713 |
MOD_Cter_Amidation | 214 | 217 | PF01082 | 0.479 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.441 |
MOD_GlcNHglycan | 15 | 19 | PF01048 | 0.663 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.516 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.496 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.387 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.494 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.571 |
MOD_GlcNHglycan | 435 | 439 | PF01048 | 0.543 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.764 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.582 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.509 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.521 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.440 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.715 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.792 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.594 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.697 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.758 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.748 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.477 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.544 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.330 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.502 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.577 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.483 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.534 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.540 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.403 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.353 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.476 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.598 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.513 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.596 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.717 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.594 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.529 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.514 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.439 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.763 |
MOD_PK_1 | 220 | 226 | PF00069 | 0.727 |
MOD_PK_1 | 385 | 391 | PF00069 | 0.563 |
MOD_PKA_1 | 422 | 428 | PF00069 | 0.646 |
MOD_PKA_1 | 433 | 439 | PF00069 | 0.683 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.500 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.519 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.694 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.564 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.713 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.612 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.613 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.435 |
MOD_PKB_1 | 447 | 455 | PF00069 | 0.598 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.463 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.583 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.645 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.397 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.360 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.565 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.563 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.727 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.629 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.604 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.608 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.692 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.490 |
TRG_DiLeu_BaEn_1 | 63 | 68 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_2 | 311 | 317 | PF01217 | 0.732 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.570 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.752 |
TRG_NES_CRM1_1 | 158 | 169 | PF08389 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 337 | 342 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRT1 | Leptomonas seymouri | 52% | 100% |
A0A3S7X756 | Leishmania donovani | 86% | 100% |
A4HLZ7 | Leishmania braziliensis | 67% | 97% |
A4I9C7 | Leishmania infantum | 86% | 100% |
Q4Q3P9 | Leishmania major | 86% | 100% |