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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4IDX4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.753 |
CLV_PCSK_FUR_1 | 316 | 320 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.702 |
CLV_PCSK_PC7_1 | 23 | 29 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.678 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.538 |
DEG_APCC_DBOX_1 | 228 | 236 | PF00400 | 0.480 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.683 |
DEG_SPOP_SBC_1 | 523 | 527 | PF00917 | 0.565 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.726 |
DOC_CYCLIN_RxL_1 | 227 | 237 | PF00134 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 152 | 155 | PF00134 | 0.585 |
DOC_CYCLIN_yCln2_LP_2 | 283 | 289 | PF00134 | 0.482 |
DOC_CYCLIN_yCln2_LP_2 | 427 | 433 | PF00134 | 0.543 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.754 |
DOC_MAPK_gen_1 | 447 | 454 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 503 | 513 | PF00069 | 0.444 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.471 |
DOC_SPAK_OSR1_1 | 172 | 176 | PF12202 | 0.718 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.679 |
DOC_USP7_UBL2_3 | 65 | 69 | PF12436 | 0.734 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.794 |
LIG_14-3-3_CanoR_1 | 16 | 25 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 191 | 198 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 360 | 364 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.525 |
LIG_Actin_WH2_2 | 490 | 505 | PF00022 | 0.492 |
LIG_BIR_III_2 | 34 | 38 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 518 | 522 | PF00533 | 0.478 |
LIG_CSL_BTD_1 | 9 | 12 | PF09270 | 0.724 |
LIG_EH1_1 | 328 | 336 | PF00400 | 0.538 |
LIG_eIF4E_1 | 329 | 335 | PF01652 | 0.462 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.570 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.521 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.628 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.526 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.721 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.566 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.510 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.785 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.723 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.452 |
LIG_Pex14_1 | 10 | 14 | PF04695 | 0.648 |
LIG_RPA_C_Fungi | 24 | 36 | PF08784 | 0.690 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 551 | 555 | PF00017 | 0.577 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.545 |
LIG_SH3_2 | 183 | 188 | PF14604 | 0.709 |
LIG_SH3_2 | 63 | 68 | PF14604 | 0.699 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.613 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.679 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.710 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.783 |
LIG_SH3_4 | 65 | 72 | PF00018 | 0.651 |
LIG_SUMO_SIM_par_1 | 299 | 308 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 456 | 462 | PF11976 | 0.429 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.555 |
LIG_TYR_ITIM | 321 | 326 | PF00017 | 0.492 |
LIG_WW_3 | 185 | 189 | PF00397 | 0.773 |
MOD_CDK_SPK_2 | 8 | 13 | PF00069 | 0.728 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.658 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.633 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.727 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.431 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.718 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.827 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.708 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.632 |
MOD_DYRK1A_RPxSP_1 | 387 | 391 | PF00069 | 0.627 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.558 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.640 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.724 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.563 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.656 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.563 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.687 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.685 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.507 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.729 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.770 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.574 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.800 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.704 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.700 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.521 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.455 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.512 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.443 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.740 |
MOD_LATS_1 | 374 | 380 | PF00433 | 0.515 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.650 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.464 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.576 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.418 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.566 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.522 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.508 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.441 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.565 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.491 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.642 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.574 |
MOD_PK_1 | 327 | 333 | PF00069 | 0.479 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.748 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.518 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.707 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.433 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.481 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.514 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.605 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.698 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.712 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.613 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.564 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.721 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.667 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.772 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.665 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.793 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_2 | 427 | 433 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_2 | 488 | 494 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.559 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.583 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 316 | 319 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.600 |
TRG_NLS_MonoExtC_3 | 26 | 31 | PF00514 | 0.713 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMS8 | Leptomonas seymouri | 45% | 95% |
A0A1X0P1C1 | Trypanosomatidae | 28% | 100% |
A0A3Q8IJU5 | Leishmania donovani | 99% | 100% |
A4HQ76 | Leishmania braziliensis | 73% | 98% |
E9ATZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q0K1 | Leishmania major | 90% | 100% |