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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7X9F0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.674 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.571 |
CLV_PCSK_FUR_1 | 397 | 401 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.641 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.583 |
DEG_SCF_FBW7_1 | 513 | 518 | PF00400 | 0.594 |
DOC_ANK_TNKS_1 | 450 | 457 | PF00023 | 0.674 |
DOC_CYCLIN_RxL_1 | 234 | 245 | PF00134 | 0.574 |
DOC_CYCLIN_yClb1_LxF_4 | 332 | 337 | PF00134 | 0.416 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 397 | 407 | PF00069 | 0.567 |
DOC_MAPK_JIP1_4 | 237 | 243 | PF00069 | 0.567 |
DOC_MAPK_MEF2A_6 | 202 | 211 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 235 | 243 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 332 | 338 | PF00149 | 0.416 |
DOC_PP2B_LxvP_1 | 447 | 450 | PF13499 | 0.672 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.466 |
DOC_WD40_RPTOR_TOS_1 | 37 | 43 | PF00400 | 0.577 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 168 | 178 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 334 | 338 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 537 | 554 | PF00022 | 0.507 |
LIG_APCC_ABBA_1 | 109 | 114 | PF00400 | 0.482 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.502 |
LIG_BIR_III_2 | 222 | 226 | PF00653 | 0.631 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.683 |
LIG_deltaCOP1_diTrp_1 | 262 | 271 | PF00928 | 0.452 |
LIG_eIF4E_1 | 136 | 142 | PF01652 | 0.555 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.548 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.549 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.559 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.637 |
LIG_FHA_2 | 541 | 547 | PF00498 | 0.515 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.508 |
LIG_LIR_Gen_1 | 156 | 167 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 269 | 278 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 491 | 501 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.584 |
LIG_MYND_1 | 470 | 474 | PF01753 | 0.632 |
LIG_NRBOX | 403 | 409 | PF00104 | 0.561 |
LIG_Pex14_1 | 264 | 268 | PF04695 | 0.430 |
LIG_Pex14_2 | 46 | 50 | PF04695 | 0.471 |
LIG_SH2_SRC | 220 | 223 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.503 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.461 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.515 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.529 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.679 |
LIG_Sin3_3 | 205 | 212 | PF02671 | 0.548 |
LIG_SUMO_SIM_anti_2 | 409 | 417 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 239 | 245 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 532 | 540 | PF11976 | 0.505 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.538 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.711 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.593 |
LIG_UBA3_1 | 404 | 411 | PF00899 | 0.577 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.672 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.649 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.459 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.595 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.622 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.631 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.627 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.672 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.699 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.553 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.544 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.637 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.603 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.591 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.484 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.471 |
MOD_DYRK1A_RPxSP_1 | 552 | 556 | PF00069 | 0.551 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.565 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.679 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.632 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.592 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.508 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.629 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.543 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.541 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.454 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.592 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.698 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.518 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.653 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.637 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.649 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.498 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.495 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.575 |
MOD_N-GLC_2 | 529 | 531 | PF02516 | 0.483 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.592 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.469 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.559 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.553 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.600 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.622 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.542 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.544 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.595 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.739 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.570 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.539 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.662 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.481 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.459 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.603 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.740 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.454 |
MOD_Plk_1 | 536 | 542 | PF00069 | 0.579 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.610 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.485 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.565 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.497 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.537 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.601 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.455 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.636 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.663 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.637 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.648 |
MOD_SUMO_rev_2 | 38 | 46 | PF00179 | 0.609 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.563 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.480 |
TRG_NES_CRM1_1 | 114 | 129 | PF08389 | 0.459 |
TRG_NES_CRM1_1 | 403 | 417 | PF08389 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 139 | 144 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.626 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Q6 | Leptomonas seymouri | 40% | 89% |
A4HMV0 | Leishmania braziliensis | 71% | 100% |
A4IBH2 | Leishmania infantum | 100% | 100% |
E9AFA7 | Leishmania major | 87% | 100% |
E9B6G2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |