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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4Q4R7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 176 | 180 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.697 |
CLV_PCSK_FUR_1 | 403 | 407 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.701 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.676 |
DEG_MDM2_SWIB_1 | 220 | 228 | PF02201 | 0.578 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.643 |
DOC_MAPK_MEF2A_6 | 165 | 173 | PF00069 | 0.544 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.549 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.659 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.561 |
LIG_14-3-3_CanoR_1 | 122 | 132 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 270 | 274 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 439 | 444 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 68 | 75 | PF00244 | 0.603 |
LIG_Actin_WH2_2 | 156 | 174 | PF00022 | 0.587 |
LIG_Actin_WH2_2 | 215 | 231 | PF00022 | 0.510 |
LIG_BIR_III_2 | 93 | 97 | PF00653 | 0.542 |
LIG_Clathr_ClatBox_1 | 219 | 223 | PF01394 | 0.502 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 223 | 227 | PF00928 | 0.439 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.618 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.479 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.507 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.577 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.706 |
LIG_GBD_Chelix_1 | 206 | 214 | PF00786 | 0.589 |
LIG_GBD_Chelix_1 | 53 | 61 | PF00786 | 0.599 |
LIG_LIR_Gen_1 | 223 | 232 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 223 | 227 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.506 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.477 |
LIG_PDZ_Class_1 | 439 | 444 | PF00595 | 0.602 |
LIG_Pex14_1 | 213 | 217 | PF04695 | 0.579 |
LIG_Pex14_2 | 217 | 221 | PF04695 | 0.563 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.564 |
LIG_SH2_STAT3 | 299 | 302 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.582 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.610 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.653 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.562 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.601 |
LIG_UBA3_1 | 45 | 52 | PF00899 | 0.499 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.470 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.655 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.559 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.614 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.694 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.475 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.647 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.590 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.633 |
MOD_Cter_Amidation | 353 | 356 | PF01082 | 0.563 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.622 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.703 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.477 |
MOD_GlcNHglycan | 156 | 160 | PF01048 | 0.635 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.500 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.587 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.613 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.615 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.669 |
MOD_GlcNHglycan | 382 | 386 | PF01048 | 0.657 |
MOD_GlcNHglycan | 422 | 426 | PF01048 | 0.589 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.635 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.694 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.637 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.693 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.633 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.549 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.609 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.735 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.604 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.689 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.545 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.584 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.679 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.556 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.599 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.527 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.543 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.608 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.659 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.579 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.705 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.657 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.563 |
MOD_PKA_1 | 254 | 260 | PF00069 | 0.605 |
MOD_PKA_1 | 320 | 326 | PF00069 | 0.647 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.774 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.606 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.497 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.512 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.624 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.551 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.647 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.643 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.608 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.572 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.651 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.638 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.749 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.660 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.668 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.561 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.606 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 367 | 370 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 438 | 441 | PF00400 | 0.639 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7T2 | Leishmania donovani | 83% | 100% |
A4HKZ5 | Leishmania braziliensis | 58% | 99% |
A4I8H5 | Leishmania infantum | 83% | 100% |
E9B3D5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |