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: E9B4X6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.693 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.616 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.645 |
DEG_APCC_KENBOX_2 | 260 | 264 | PF00400 | 0.592 |
DEG_SCF_FBW7_2 | 6 | 11 | PF00400 | 0.553 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.649 |
DEG_SPOP_SBC_1 | 205 | 209 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 422 | 426 | PF00917 | 0.602 |
DOC_CYCLIN_RxL_1 | 475 | 486 | PF00134 | 0.499 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 144 | 153 | PF00134 | 0.577 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.592 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.551 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.762 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 360 | 364 | PF00244 | 0.647 |
LIG_APCC_ABBA_1 | 15 | 20 | PF00400 | 0.617 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.662 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.619 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.679 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.528 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.625 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.601 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.618 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.751 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.503 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.505 |
LIG_LIR_Gen_1 | 103 | 110 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.590 |
LIG_LRP6_Inhibitor_1 | 341 | 347 | PF00058 | 0.488 |
LIG_PCNA_PIPBox_1 | 484 | 493 | PF02747 | 0.508 |
LIG_PCNA_yPIPBox_3 | 478 | 491 | PF02747 | 0.459 |
LIG_PTB_Apo_2 | 381 | 388 | PF02174 | 0.604 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.614 |
LIG_SH2_GRB2like | 105 | 108 | PF00017 | 0.685 |
LIG_SH2_NCK_1 | 105 | 109 | PF00017 | 0.577 |
LIG_SH2_STAT3 | 382 | 385 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.589 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.635 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.556 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.634 |
LIG_SUMO_SIM_par_1 | 207 | 215 | PF11976 | 0.548 |
LIG_TRAF2_1 | 383 | 386 | PF00917 | 0.630 |
LIG_TYR_ITSM | 101 | 108 | PF00017 | 0.502 |
LIG_WRC_WIRS_1 | 328 | 333 | PF05994 | 0.663 |
MOD_CDC14_SPxK_1 | 135 | 138 | PF00782 | 0.714 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.713 |
MOD_CDK_SPxK_1 | 273 | 279 | PF00069 | 0.552 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.611 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.678 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.541 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.559 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.607 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.616 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.782 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.633 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.672 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.608 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.650 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.622 |
MOD_GlcNHglycan | 11 | 15 | PF01048 | 0.628 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.611 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.627 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.557 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.604 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.783 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.670 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.583 |
MOD_GlcNHglycan | 501 | 505 | PF01048 | 0.459 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.714 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.704 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.650 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.573 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.513 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.634 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.559 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.766 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.515 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.565 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.642 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.706 |
MOD_LATS_1 | 421 | 427 | PF00433 | 0.703 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.686 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.618 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.742 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.511 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.542 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.585 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.733 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.585 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.575 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.550 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.490 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.503 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.652 |
MOD_NEK2_2 | 355 | 360 | PF00069 | 0.615 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.677 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.529 |
MOD_PK_1 | 221 | 227 | PF00069 | 0.521 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.656 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.648 |
MOD_PKB_1 | 178 | 186 | PF00069 | 0.601 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.540 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.687 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.613 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.510 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.529 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.648 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.617 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.462 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.461 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.628 |
MOD_Plk_2-3 | 125 | 131 | PF00069 | 0.620 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.695 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.597 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.607 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.538 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.602 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.668 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.637 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.552 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.709 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.763 |
MOD_SUMO_rev_2 | 67 | 73 | PF00179 | 0.514 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 415 | 421 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.613 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 37 | 39 | PF00400 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 265 | 270 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 478 | 483 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8X2 | Leptomonas seymouri | 55% | 92% |
A0A3S7X7T0 | Leishmania donovani | 91% | 100% |
A4H7S3 | Leishmania braziliensis | 76% | 100% |
A4I9W3 | Leishmania infantum | 92% | 100% |
Q4Q351 | Leishmania major | 91% | 100% |